Variant report

Variant	esv1816376
Chromosome Location	chr4:70013842-70307274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1966)
CpG islands
(count:306)
Chromatin interactive
region (count:21)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1966 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:70045525-70045926	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:70047409-70047599	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:70036297-70036563	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:70210667-70210694	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:70018787-70019146	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:70296492-70296914	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:70296492-70296919	K562	blood:	n/a	n/a
8	ARID3A	chr4:70056442-70056604	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:70106482-70106878	HepG2	liver:	n/a	n/a
10	ARID3A	chr4:70105540-70105900	HepG2	liver:	n/a	n/a
11	ARID3A	chr4:70105523-70105754	K562	blood:	n/a	n/a
12	ARID3A	chr4:70274315-70274516	HepG2	liver:	n/a	n/a
13	ARID3A	chr4:70080605-70080753	HepG2	liver:	n/a	n/a
14	ARID3A	chr4:70254846-70255212	HepG2	liver:	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	chr4:70105493-70105808	K562	blood:	n/a	n/a
20	ATF1	chr4:70033053-70033356	K562	blood:	n/a	n/a
21	ATF1	chr4:70175307-70175700	K562	blood:	n/a	n/a
22	ATF2	chr4:70033061-70033352	GM12878	blood:	n/a	n/a
23	ATF2	chr4:70032979-70033329	GM12878	blood:	n/a	n/a
24	ATF3	chr4:70296558-70296973	A549	lung:	n/a	n/a
25	ATF3	chr4:70296574-70296796	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF3	chr4:70296552-70296826	A549	lung:	n/a	n/a
27	ATF3	chr4:70296499-70296777	HepG2	liver:	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	BACH1	chr4:70097393-70097475	K562	blood:	n/a	n/a
32	BATF	chr4:70296590-70296824	GM12878	blood:	n/a	n/a
33	BATF	chr4:70033033-70033336	GM12878	blood:	n/a	chr4:70033221-70033232
34	BATF	chr4:70296589-70296863	GM12878	blood:	n/a	chr4:70296823-70296832
35	BCL11A	chr4:70296596-70296779	GM12878	blood:	n/a	n/a
36	BCL11A	chr4:70296551-70296867	GM12878	blood:	n/a	n/a
37	BCL11A	chr4:70296569-70296786	H1-hESC	embryonic stem cell:	n/a	n/a
38	BCL11A	chr4:70296603-70296770	H1-hESC	embryonic stem cell:	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	BCL3	chr4:70296436-70296843	A549	lung:	n/a	n/a
42	BCLAF1	chr4:70296549-70296826	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:70044628-70044869	K562	blood:	n/a	n/a
44	BHLHE40	chr4:70209675-70209715	K562	blood:	n/a	n/a
45	BHLHE40	chr4:70057696-70057810	K562	blood:	n/a	n/a
46	BHLHE40	chr4:70047447-70047661	HepG2	liver:	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	chr4:70105574-70105707	K562	blood:	n/a	n/a
50	BHLHE40	chr4:70296485-70296909	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	chr4:70155747-70155797	SK-N-SH_RA	brain:	n/a
2	chr4:70155747-70155797	SK-N-SH_RA	brain:	n/a
3	chr4:70155747-70155797	NHBE	bronchial:	n/a
4	chr4:70155747-70155797	AG04450	lung:	fetal
5	chr4:70065325-70065375	NB4	blood:	n/a
6	chr4:70080453-70080503	SAEC	small airway:	n/a
7	chr4:70080453-70080503	HRE	kidney:	n/a
8	chr4:70080453-70080503	GM06990	blood:	n/a
9	chr4:70080453-70080503	IMR90	lung:	fetal
10	chr4:70065325-70065375	Caco-2	colon:	n/a
11	chr4:70155747-70155797	U87	brain:	n/a
12	chr4:70080453-70080503	HEK293	kidney:	embryo
13	chr4:70064835-70064885	HNPCEpiC	eye:	n/a
14	chr4:70155747-70155797	MCF-7	breast:	n/a
15	chr4:70066318-70066368	HCM	heart:	n/a
16	chr4:70065325-70065375	U87	brain:	n/a
17	chr4:70155747-70155797	LNCaP	prostate:	n/a
18	chr4:70155747-70155797	SAEC	small airway:	n/a
19	chr4:70155747-70155797	IMR90	lung:	fetal
20	chr4:70066318-70066368	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:70064835-70064885	AG04450	lung:	fetal
22	chr4:70064835-70064885	SAEC	small airway:	n/a
23	chr4:70066318-70066368	SK-N-SH	brain:	n/a
24	chr4:70080453-70080503	MCF10A-Er-Src	breast:	n/a
25	chr4:70066318-70066368	U87	brain:	n/a
26	chr4:70155747-70155797	AG09319	gingival:	n/a
27	chr4:70065325-70065375	PrEC	prostate:	n/a
28	chr4:70080453-70080503	HAEpiC	amniotic membrane:	n/a
29	chr4:70155747-70155797	NT2-D1	testis:	n/a
30	chr4:70065325-70065375	GM12892	blood:	n/a
31	chr4:70066318-70066368	AG09309	skin:	n/a
32	chr4:70066318-70066368	HepG2	liver:	n/a
33	chr4:70065325-70065375	SK-N-SH	brain:	n/a
34	chr4:70064835-70064885	HIPEpiC	eye:	n/a
35	chr4:70065325-70065375	HMEC	breast:	n/a
36	chr4:70155747-70155797	GM12878	blood:	n/a
37	chr4:70065325-70065375	ECC-1	luminal epithelium:	n/a
38	chr4:70155747-70155797	ECC-1	luminal epithelium:	n/a
39	chr4:70080453-70080503	HEEpiC	esophagus:	n/a
40	chr4:70066318-70066368	HMEC	breast:	n/a
41	chr4:70155747-70155797	HCF	heart:	n/a
42	chr4:70065325-70065375	PANC-1	pancreas:	n/a
43	chr4:70065325-70065375	PFSK-1	brain:	n/a
44	chr4:70064835-70064885	NB4	blood:	n/a
45	chr4:70064835-70064885	PANC-1	pancreas:	n/a
46	chr4:70065325-70065375	AG09309	skin:	n/a
47	chr4:70080453-70080503	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:70066318-70066368	GM12891	blood:	n/a
49	chr4:70064835-70064885	BJ	skin:	n/a
50	chr4:70066318-70066368	GM19239	blood:	n/a

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

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

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B28-4	chr4:70253298-70254025	NONHSAT096763
2	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
3	lnc-UGT2B28-1	chr4:70066890-70067002	ENSG00000250696.1
4	lnc-UGT2B28-1	chr4:70047818-70048090	ENSG00000250696.1
5	lnc-UGT2B28-1	chr4:70080191-70082484	ENSG00000250696.1
6	lnc-UGT2B28-1	chr4:70047378-70048090	NONHSAT096756
7	lnc-UGT2B28-1	chr4:70066138-70066296	ENSG00000250696.1
8	lnc-UGT2B28-5	chr4:70272649-70273373	NONHSAT096764
9	lnc-UGT2B28-1	chr4:70061386-70061489	ENSG00000250696.1
10	lnc-UGT2B28-6	chr4:70306600-70306768	NONHSAT096765
11	lnc-UGT2B28-6	chr4:70303075-70303156	NONHSAT096765
12	lnc-UGT2B28-6	chr4:70304044-70304260	NONHSAT096765
13	lnc-UGT2B28-1	chr4:70076784-70076865	ENSG00000250696.1
14	lnc-UGT2B28-1	chr4:70080191-70080193	ENSG00000250696.1
15	lnc-UGT2B28-1	chr4:70066190-70066296	ENSG00000250696.1

No data

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

Extended variants
information (count: 5313 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:5313 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189146597	chr4:70018430-70018431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74681218	chr4:70018471-70018472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552664898	chr4:70018509-70018510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11936906	chr4:70018525-70018526	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs368993846	chr4:70018553-70018554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528508480	chr4:70018580-70018581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs386675650	chr4:70018582-70018583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372283643	chr4:70018587-70018588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568365321	chr4:70018599-70018600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs192147942	chr4:70018612-70018613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373178725	chr4:70018618-70018619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7671653	chr4:70018645-70018646	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs76083041	chr4:70018651-70018652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539138719	chr4:70018668-70018669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76617299	chr4:70018671-70018672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572472978	chr4:70018682-70018683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535104839	chr4:70018690-70018691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184524268	chr4:70018737-70018738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574803554	chr4:70018757-70018758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544139061	chr4:70018761-70018762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146684700	chr4:70018802-70018803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs76843910	chr4:70018808-70018809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74922037	chr4:70018814-70018815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545941487	chr4:70018905-70018906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548763265	chr4:70018913-70018914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs145042691	chr4:70018935-70018936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs528446618	chr4:70018966-70018967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548611642	chr4:70018984-70018985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562105344	chr4:70018985-70018986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565673109	chr4:70019009-70019010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75988947	chr4:70019061-70019062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550880745	chr4:70019099-70019100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570540112	chr4:70019132-70019133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140515451	chr4:70019271-70019272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376660843	chr4:70019274-70019275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74647941	chr4:70019277-70019278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35264089	chr4:70019288-70019289	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs13134261	chr4:70019333-70019334	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs554936302	chr4:70019338-70019339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574919394	chr4:70019370-70019371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12647599	chr4:70019396-70019397	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs187131690	chr4:70019446-70019447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201820513	chr4:70019451-70019452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139604634	chr4:70019452-70019453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577337288	chr4:70019474-70019475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546379806	chr4:70019494-70019495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553462794	chr4:70019542-70019543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573365769	chr4:70019546-70019547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191951455	chr4:70019613-70019614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562041644	chr4:70019683-70019684	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:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:70018400-70019400	Enhancers	Liver	Liver
2	chr4:70018600-70019400	Enhancers	HepG2	liver
3	chr4:70019400-70031200	Weak transcription	HepG2	liver
4	chr4:70025800-70026200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:70030600-70031400	Enhancers	Rectal Smooth Muscle	rectum
6	chr4:70031200-70031400	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr4:70031200-70032600	Enhancers	HepG2	liver
8	chr4:70031400-70032600	Enhancers	Fetal Intestine Large	intestine
9	chr4:70031600-70031800	Enhancers	Liver	Liver
10	chr4:70031800-70035400	Active TSS	Liver	Liver
11	chr4:70032200-70032600	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr4:70032600-70035400	Weak transcription	HepG2	liver
13	chr4:70035000-70035200	ZNF genes & repeats	Fetal Intestine Small	intestine
14	chr4:70035200-70043600	Weak transcription	Fetal Intestine Small	intestine
15	chr4:70035400-70035800	Flanking Active TSS	Liver	Liver
16	chr4:70035400-70036400	Enhancers	HepG2	liver
17	chr4:70035800-70038200	Enhancers	Liver	Liver
18	chr4:70038200-70038600	Weak transcription	Liver	Liver
19	chr4:70038600-70038800	Enhancers	Liver	Liver
20	chr4:70038800-70041000	Weak transcription	Liver	Liver
21	chr4:70041000-70042000	Strong transcription	Liver	Liver
22	chr4:70042000-70044400	Weak transcription	Liver	Liver
23	chr4:70043600-70043800	Enhancers	Fetal Intestine Large	intestine
24	chr4:70043600-70044800	Enhancers	Fetal Intestine Small	intestine
25	chr4:70043600-70045600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr4:70043800-70044800	Weak transcription	Fetal Intestine Large	intestine
27	chr4:70044000-70044600	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr4:70044200-70044400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:70044400-70044600	Enhancers	Liver	Liver
30	chr4:70044400-70045000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr4:70044400-70045400	Enhancers	Stomach Mucosa	stomach
32	chr4:70044600-70045000	Flanking Active TSS	Liver	Liver
33	chr4:70044800-70045000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:70044800-70045200	Enhancers	Primary B cells from peripheral blood	blood
35	chr4:70044800-70045400	Flanking Active TSS	Fetal Intestine Small	intestine
36	chr4:70044800-70045600	Enhancers	Fetal Intestine Large	intestine
37	chr4:70045000-70045200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr4:70045000-70045200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr4:70045000-70045600	Enhancers	Duodenum Mucosa	Duodenum
40	chr4:70045000-70045600	Enhancers	HepG2	liver
41	chr4:70045000-70045800	Enhancers	Primary hematopoietic stem cells	blood
42	chr4:70045000-70046200	Enhancers	Liver	Liver
43	chr4:70045200-70046200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:70045200-70047400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:70045400-70045600	Enhancers	Fetal Intestine Small	intestine
46	chr4:70045600-70046600	Weak transcription	HepG2	liver
47	chr4:70046200-70047400	Weak transcription	Liver	Liver
48	chr4:70046600-70046800	Enhancers	HepG2	liver
49	chr4:70046800-70047400	Weak transcription	HepG2	liver
50	chr4:70047200-70048000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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