Variant report

Variant	esv3518601
Chromosome Location	chr4:81523238-81831941
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:962)
CpG islands
(count:61)
Chromatin interactive
region (count:30)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:81540306-81540462	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:81536315-81536564	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:81540281-81540488	K562	blood:	n/a	n/a
4	ATF2	chr4:81797888-81798408	GM12878	blood:	n/a	n/a
5	ATF2	chr4:81763026-81763419	GM12878	blood:	n/a	n/a
6	ATF2	chr4:81796730-81797216	GM12878	blood:	n/a	n/a
7	ATF2	chr4:81797799-81798459	GM12878	blood:	n/a	n/a
8	ATF2	chr4:81796747-81797219	GM12878	blood:	n/a	n/a
9	BACH1	chr4:81631922-81632282	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:81672435-81672720	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:81763070-81763363	GM12878	blood:	n/a	n/a
12	BATF	chr4:81796744-81797221	GM12878	blood:	n/a	n/a
13	BATF	chr4:81711363-81711557	GM12878	blood:	n/a	chr4:81711432-81711440
14	BATF	chr4:81797909-81798372	GM12878	blood:	n/a	n/a
15	BATF	chr4:81797914-81798369	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:81763125-81763395	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:81796748-81797201	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:81797973-81798345	GM12878	blood:	n/a	chr4:81798148-81798157
19	BCL11A	chr4:81646559-81646736	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr4:81797887-81798401	GM12878	blood:	n/a	chr4:81798148-81798157
21	BCL11A	chr4:81532131-81532308	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:81532008-81532366	GM12878	blood:	n/a	n/a
23	BCL3	chr4:81797868-81798380	GM12878	blood:	n/a	chr4:81798148-81798157
24	BCL3	chr4:81797892-81798328	GM12878	blood:	n/a	chr4:81798148-81798157
25	BCLAF1	chr4:81797918-81798340	GM12878	blood:	n/a	chr4:81798148-81798157
26	BCLAF1	chr4:81796774-81797043	GM12878	blood:	n/a	n/a
27	BCLAF1	chr4:81797821-81798479	GM12878	blood:	n/a	chr4:81798148-81798157
28	BCLAF1	chr4:81796740-81797149	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:81531862-81532820	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:81796831-81797153	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:81798003-81798335	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:81533942-81534173	GM12878	blood:	n/a	n/a
33	CCNT2	chr4:81735997-81736139	K562	blood:	n/a	n/a
34	CCNT2	chr4:81569268-81569430	K562	blood:	n/a	n/a
35	CEBPB	chr4:81785180-81785397	IMR90	lung:	n/a	chr4:81785241-81785252
36	CEBPB	chr4:81799398-81799775	IMR90	lung:	n/a	chr4:81799582-81799593
37	CEBPB	chr4:81576458-81576621	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:81785103-81785397	HepG2	liver:	n/a	chr4:81785241-81785252
39	CEBPB	chr4:81607266-81607495	IMR90	lung:	n/a	chr4:81607359-81607372 chr4:81607361-81607372
40	CEBPB	chr4:81796625-81797217	GM12878	blood:	n/a	n/a
41	CEBPB	chr4:81785155-81785315	K562	blood:	n/a	chr4:81785241-81785252
42	CEBPB	chr4:81752924-81753282	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:81762891-81763480	GM12878	blood:	n/a	chr4:81763334-81763345 chr4:81763333-81763346
44	CEBPB	chr4:81649175-81649482	HepG2	liver:	n/a	chr4:81649334-81649347 chr4:81649334-81649345 chr4:81649336-81649347 chr4:81649336-81649345
45	CEBPB	chr4:81627081-81627293	H1-hESC	embryonic stem cell:	n/a	chr4:81627168-81627179 chr4:81627168-81627181 chr4:81627169-81627180 chr4:81627168-81627181
46	CEBPB	chr4:81534827-81535128	HepG2	liver:	n/a	chr4:81534961-81534972 chr4:81534959-81534970
47	CEBPB	chr4:81626994-81627342	HepG2	liver:	n/a	chr4:81627168-81627179 chr4:81627168-81627181 chr4:81627169-81627180 chr4:81627168-81627181
48	CEBPB	chr4:81797837-81798442	GM12878	blood:	n/a	chr4:81798354-81798365 chr4:81798354-81798367 chr4:81798354-81798365
49	CEBPB	chr4:81626996-81627300	IMR90	lung:	n/a	chr4:81627168-81627179 chr4:81627168-81627181 chr4:81627169-81627180 chr4:81627168-81627181
50	CEBPB	chr4:81799447-81799701	H1-hESC	embryonic stem cell:	n/a	chr4:81799582-81799593

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:81660494-81660544	SK-N-SH	brain:	n/a
2	chr4:81660494-81660544	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:81660494-81660544	GM12892	blood:	n/a
4	chr4:81660494-81660544	NH-A	brain:	n/a
5	chr4:81660494-81660544	HRE	kidney:	n/a
6	chr4:81660494-81660544	CMK	blood:	n/a
7	chr4:81660494-81660544	HRPEpiC	eye:	n/a
8	chr4:81660494-81660544	Hela-S3	cervix:	n/a
9	chr4:81660494-81660544	GM19239	blood:	n/a
10	chr4:81660494-81660544	H1-hESC	embryonic stem cell:	embryo
11	chr4:81660494-81660544	NB4	blood:	n/a
12	chr4:81660494-81660544	SKMC	muscle:	n/a
13	chr4:81660494-81660544	GM06990	blood:	n/a
14	chr4:81660494-81660544	HCT-116	colon:	n/a
15	chr4:81660494-81660544	AG04449	skin:	fetal
16	chr4:81660494-81660544	HEK293	kidney:	embryo
17	chr4:81660494-81660544	HRCEpiC	kidney:	n/a
18	chr4:81660494-81660544	HMEC	breast:	n/a
19	chr4:81660494-81660544	ECC-1	luminal epithelium:	n/a
20	chr4:81660494-81660544	MCF10A-Er-Src	breast:	n/a
21	chr4:81660494-81660544	RPTEC	kidney:	n/a
22	chr4:81660494-81660544	NHDF-neo	bronchial:	n/a
23	chr4:81660494-81660544	PFSK-1	brain:	n/a
24	chr4:81660494-81660544	SK-N-MC	brain:	n/a
25	chr4:81660494-81660544	MCF-7	breast:	n/a
26	chr4:81660494-81660544	PrEC	prostate:	n/a
27	chr4:81660494-81660544	AG04450	lung:	fetal
28	chr4:81660494-81660544	PANC-1	pancreas:	n/a
29	chr4:81660494-81660544	A549	lung:	n/a
30	chr4:81660494-81660544	AG09309	skin:	n/a
31	chr4:81660494-81660544	GM12891	blood:	n/a
32	chr4:81660494-81660544	AoSMC	blood vessel:	n/a
33	chr4:81660494-81660544	HL-60	blood:	n/a
34	chr4:81660494-81660544	K562	blood:	n/a
35	chr4:81660494-81660544	BE2_C	brain:	n/a
36	chr4:81660494-81660544	SAEC	small airway:	n/a
37	chr4:81660494-81660544	HCM	heart:	n/a
38	chr4:81660494-81660544	NT2-D1	testis:	n/a
39	chr4:81660494-81660544	HIPEpiC	eye:	n/a
40	chr4:81660494-81660544	ovcar-3	ovarian:	n/a
41	chr4:81660494-81660544	GM12878	blood:	n/a
42	chr4:81660494-81660544	U87	brain:	n/a
43	chr4:81660494-81660544	LNCaP	prostate:	n/a
44	chr4:81660494-81660544	HUVEC	blood vessel:	n/a
45	chr4:81660494-81660544	HNPCEpiC	eye:	n/a
46	chr4:81660494-81660544	HCPEpiC	choroid plexus:	n/a
47	chr4:81660494-81660544	Hepatocyte	liver:	n/a
48	chr4:81660494-81660544	AG10803	skin:	n/a
49	chr4:81660494-81660544	HAEpiC	amniotic membrane:	n/a
50	chr4:81660494-81660544	HEEpiC	esophagus:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:81539992..81540886-chr4:81910834..81911713,5	MCF-7	breast:
2	chr4:81756515..81759052-chr4:81760734..81762863,2	K562	blood:
3	chr4:81726557..81729431-chr4:81734231..81736856,2	MCF-7	breast:
4	chr4:81732367..81734767-chr4:81734914..81738399,4	K562	blood:
5	chr4:81726557..81729431-chr4:81734231..81736856,2	MCF-7	breast:
6	chr4:81624160..81627209-chr4:81627794..81630276,3	K562	blood:
7	chr20:5429160..5429789-chr4:81671748..81672503,2	MCF-7	breast:
8	chr4:81675024..81677114-chr4:81678812..81680494,2	K562	blood:
9	chr4:81286836..81287415-chr4:81540565..81541217,2	MCF-7	breast:
10	chr4:81624160..81627209-chr4:81627794..81630276,3	K562	blood:
11	chr4:81794667..81796938-chr4:81800579..81802304,2	K562	blood:
12	chr4:81789838..81792795-chr4:81793181..81795732,2	MCF-7	breast:
13	chr4:81756515..81759052-chr4:81760734..81762863,2	K562	blood:
14	chr4:81667228..81669578-chr4:81671291..81673387,2	MCF-7	breast:
15	chr4:81667228..81669578-chr4:81671291..81673387,2	MCF-7	breast:
16	chr4:81732367..81734767-chr4:81734914..81738399,4	K562	blood:
17	chr4:81581396..81581979-chr4:81761045..81761732,2	MCF-7	breast:
18	chr4:81652068..81654710-chr4:81662005..81664580,2	MCF-7	breast:
19	chr4:81519146..81521026-chr4:81528690..81531037,2	MCF-7	breast:
20	chr4:81540203..81541132-chr4:81973708..81974534,2	MCF-7	breast:
21	chr4:81627156..81628838-chr4:81631785..81634489,2	K562	blood:
22	chr4:81675024..81677114-chr4:81678812..81680494,2	K562	blood:
23	chr4:81627156..81628838-chr4:81631785..81634489,2	K562	blood:
24	chr4:81794667..81796938-chr4:81800579..81802304,2	K562	blood:
25	chr4:81543453..81546267-chr4:81555168..81557103,2	MCF-7	breast:
26	chr4:81696073..81698276-chr4:81701029..81703703,2	K562	blood:
27	chr4:81652068..81654710-chr4:81662005..81664580,2	MCF-7	breast:
28	chr4:81696073..81698276-chr4:81701029..81703703,2	K562	blood:
29	chr4:81543453..81546267-chr4:81555168..81557103,2	MCF-7	breast:
30	chr4:81581396..81581979-chr4:81761045..81761732,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMP3-2	chr4:81791203-81791289	NONHSAT097143

No data

Variant related genes	Relation type
C4orf22	TF binding region
C4orf22	CpG island
ENSG00000197826	chromatin interactions

Extended variants
information (count: 3628 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3628 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56914874	chr4:81523297-81523298	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182993221	chr4:81523333-81523334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571922573	chr4:81523355-81523356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35563729	chr4:81523375-81523376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537764392	chr4:81523383-81523384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs397994198	chr4:81523386-81523387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146477040	chr4:81523472-81523473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574165468	chr4:81523478-81523479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56661575	chr4:81523503-81523504	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs553032581	chr4:81523534-81523535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140929653	chr4:81523551-81523552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544555473	chr4:81523582-81523583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575501446	chr4:81523610-81523611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534927542	chr4:81523685-81523686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558066895	chr4:81523691-81523692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187289732	chr4:81523773-81523774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs193049599	chr4:81523886-81523887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544086064	chr4:81523904-81523905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561054907	chr4:81523905-81523906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529895671	chr4:81523932-81523933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs546517953	chr4:81523933-81523934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144632881	chr4:81523944-81523945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183929660	chr4:81523976-81523977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138531719	chr4:81523983-81523984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149242517	chr4:81524017-81524018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188876457	chr4:81524023-81524024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs143842148	chr4:81524028-81524029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375617360	chr4:81524058-81524059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535876722	chr4:81524085-81524086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148160383	chr4:81524102-81524103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553291354	chr4:81524184-81524185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141963876	chr4:81524186-81524187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554232949	chr4:81524194-81524195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2867780	chr4:81524200-81524201	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs192522484	chr4:81524220-81524221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543918592	chr4:81524221-81524222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116294463	chr4:81524291-81524292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574654983	chr4:81524384-81524385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559644115	chr4:81524386-81524387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528382681	chr4:81524470-81524471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71596021	chr4:81524505-81524506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183757512	chr4:81524561-81524562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188814462	chr4:81524596-81524597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs377689769	chr4:81524604-81524605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547027939	chr4:81524629-81524630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10033938	chr4:81524630-81524631	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs565408192	chr4:81524654-81524655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116777852	chr4:81524705-81524706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550740677	chr4:81524723-81524724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567899717	chr4:81524752-81524753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Myelodysplastic syndrome	18508791	CNVD
abnormal development	18461090	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Chronic lymphocytic leukemia	21215367	CNVD
Cancer	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81511400-81529400	Weak transcription	Osteobl	bone
2	chr4:81523800-81524000	Enhancers	NH-A	brain
3	chr4:81523800-81524200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:81524200-81525600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:81525600-81525800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:81525600-81526600	Enhancers	NH-A	brain
7	chr4:81526200-81526600	Enhancers	Muscle Satellite Cultured Cells	--
8	chr4:81529000-81530600	Enhancers	Rectal Smooth Muscle	rectum
9	chr4:81529000-81530600	Enhancers	NHDF-Ad	bronchial
10	chr4:81529400-81529800	Enhancers	Duodenum Smooth Muscle	Duodenum
11	chr4:81529400-81530200	Enhancers	Fetal Intestine Large	intestine
12	chr4:81529400-81530400	Enhancers	Osteobl	bone
13	chr4:81529400-81530600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:81529400-81530600	Enhancers	Colon Smooth Muscle	Colon
15	chr4:81529600-81530600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:81530200-81530400	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr4:81530200-81531400	Weak transcription	Fetal Intestine Large	intestine
18	chr4:81530400-81531600	Weak transcription	Osteobl	bone
19	chr4:81530600-81531000	Weak transcription	Colon Smooth Muscle	Colon
20	chr4:81530600-81532000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr4:81530800-81531000	Enhancers	Primary B cells from cord blood	blood
22	chr4:81531000-81531200	Flanking Active TSS	Primary B cells from cord blood	blood
23	chr4:81531000-81531200	Enhancers	Colon Smooth Muscle	Colon
24	chr4:81531200-81531600	Enhancers	Primary B cells from cord blood	blood
25	chr4:81531200-81532400	Weak transcription	Colon Smooth Muscle	Colon
26	chr4:81531200-81533200	Enhancers	Primary B cells from peripheral blood	blood
27	chr4:81531400-81532800	Enhancers	Duodenum Mucosa	Duodenum
28	chr4:81531400-81533200	Enhancers	Fetal Intestine Large	intestine
29	chr4:81531400-81533200	Enhancers	Fetal Intestine Small	intestine
30	chr4:81531400-81533200	Enhancers	GM12878-XiMat	blood
31	chr4:81531400-81535000	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr4:81531600-81532200	Enhancers	Osteobl	bone
33	chr4:81531600-81533000	Flanking Active TSS	Primary B cells from cord blood	blood
34	chr4:81532000-81532400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr4:81532000-81532400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr4:81532000-81532400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:81532000-81532400	Enhancers	Stomach Mucosa	stomach
38	chr4:81532000-81532400	Enhancers	NHDF-Ad	bronchial
39	chr4:81532000-81532800	Enhancers	Primary T cells from cord blood	blood
40	chr4:81532000-81532800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr4:81532000-81532800	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr4:81532000-81533000	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr4:81532200-81532400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr4:81532200-81533000	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr4:81532400-81532800	Enhancers	Colon Smooth Muscle	Colon
46	chr4:81532400-81532800	Weak transcription	Stomach Mucosa	stomach
47	chr4:81532800-81533000	Flanking Active TSS	Duodenum Mucosa	Duodenum
48	chr4:81532800-81533000	Enhancers	Stomach Mucosa	stomach
49	chr4:81532800-81533200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
50	chr4:81533000-81533600	Enhancers	Primary B cells from cord blood	blood

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