Variant report

Variant	nsv879517
Chromosome Location	chr4:86677107-86739805
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:966)
CpG islands
(count:366)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:966 , 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	ATF2	chr4:86701829-86702202	GM12878	blood:	n/a	n/a
2	ATF2	chr4:86699429-86700328	GM12878	blood:	n/a	n/a
3	ATF2	chr4:86699377-86700358	GM12878	blood:	n/a	n/a
4	BACH1	chr4:86728892-86729148	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr4:86699450-86699682	GM12878	blood:	n/a	n/a
6	BATF	chr4:86699951-86700203	GM12878	blood:	n/a	n/a
7	BATF	chr4:86699863-86700245	GM12878	blood:	n/a	n/a
8	BATF	chr4:86701795-86702100	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:86699475-86699738	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:86699408-86699769	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:86701822-86702171	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:86699862-86700242	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:86699960-86700202	GM12878	blood:	n/a	n/a
14	BCL3	chr4:86720876-86721160	GM12878	blood:	n/a	n/a
15	BCLAF1	chr4:86699359-86699730	GM12878	blood:	n/a	n/a
16	BCLAF1	chr4:86699355-86699862	GM12878	blood:	n/a	n/a
17	BHLHE40	chr4:86699425-86700307	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:86718091-86718300	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:86701733-86702134	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:86717899-86718230	K562	blood:	n/a	n/a
21	BRCA1	chr4:86717947-86718272	H1-hESC	embryonic stem cell:	n/a	n/a
22	BRCA1	chr4:86717828-86718292	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr4:86697638-86698170	HCT-116	colon:	n/a	n/a
24	CCNT2	chr4:86687332-86687532	K562	blood:	n/a	n/a
25	CEBPB	chr4:86719565-86719880	HepG2	liver:	n/a	chr4:86719754-86719765 chr4:86719739-86719750
26	CEBPB	chr4:86708130-86708753	A549	lung:	n/a	chr4:86708437-86708450
27	CEBPB	chr4:86693246-86693317	K562	blood:	n/a	chr4:86693273-86693284 chr4:86693256-86693267
28	CEBPB	chr4:86708204-86708732	MCF-7	breast:	n/a	chr4:86708437-86708450
29	CEBPB	chr4:86683018-86683976	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:86699481-86699700	HepG2	liver:	n/a	chr4:86699590-86699601
31	CEBPB	chr4:86719591-86719871	Hela-S3	cervix:	n/a	chr4:86719754-86719765 chr4:86719739-86719750
32	CEBPB	chr4:86681008-86681015	K562	blood:	n/a	n/a
33	CEBPB	chr4:86708189-86708867	MCF-7	breast:	n/a	chr4:86708437-86708450
34	CEBPB	chr4:86719605-86719892	IMR90	lung:	n/a	chr4:86719754-86719765 chr4:86719739-86719750
35	CEBPB	chr4:86708281-86708714	A549	lung:	n/a	chr4:86708437-86708450
36	CEBPB	chr4:86708217-86708623	A549	lung:	n/a	chr4:86708437-86708450
37	CEBPB	chr4:86704686-86705251	IMR90	lung:	n/a	chr4:86704953-86704965
38	CEBPB	chr4:86699412-86699766	IMR90	lung:	n/a	chr4:86699590-86699601
39	CEBPB	chr4:86708240-86708759	IMR90	lung:	n/a	chr4:86708437-86708450
40	CEBPB	chr4:86708258-86708665	Hela-S3	cervix:	n/a	chr4:86708437-86708450
41	CEBPB	chr4:86679488-86679588	A549	lung:	n/a	n/a
42	CEBPB	chr4:86690148-86690183	A549	lung:	n/a	n/a
43	CEBPB	chr4:86680878-86681179	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:86718114-86718456	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:86699446-86699737	A549	lung:	n/a	chr4:86699590-86699601
46	CEBPB	chr4:86693167-86693426	HepG2	liver:	n/a	chr4:86693273-86693284 chr4:86693256-86693267
47	CEBPB	chr4:86734825-86734932	HepG2	liver:	n/a	chr4:86734894-86734905
48	CHD1	chr4:86699162-86700342	GM12878	blood:	n/a	n/a
49	CHD1	chr4:86717630-86718439	IMR90	lung:	n/a	n/a
50	CHD2	chr4:86699478-86700234	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:86699962-86700012	SK-N-MC	brain:	n/a
2	chr4:86718190-86718240	IMR90	lung:	fetal
3	chr4:86708298-86708348	SKMC	muscle:	n/a
4	chr4:86718190-86718240	LNCaP	prostate:	n/a
5	chr4:86705640-86705690	AG10803	skin:	n/a
6	chr4:86699705-86699755	NH-A	brain:	n/a
7	chr4:86705640-86705690	SK-N-MC	brain:	n/a
8	chr4:86718190-86718240	U87	brain:	n/a
9	chr4:86708298-86708348	NHDF-neo	bronchial:	n/a
10	chr4:86699705-86699755	ovcar-3	ovarian:	n/a
11	chr4:86699962-86700012	HRCEpiC	kidney:	n/a
12	chr4:86705640-86705690	PFSK-1	brain:	n/a
13	chr4:86699705-86699755	NHBE	bronchial:	n/a
14	chr4:86682649-86682699	GM12891	blood:	n/a
15	chr4:86699705-86699755	HL-60	blood:	n/a
16	chr4:86708298-86708348	MCF-7	breast:	n/a
17	chr4:86699962-86700012	AG09309	skin:	n/a
18	chr4:86682649-86682699	RPTEC	kidney:	n/a
19	chr4:86699705-86699755	GM12878	blood:	n/a
20	chr4:86699705-86699755	SAEC	small airway:	n/a
21	chr4:86699705-86699755	HRPEpiC	eye:	n/a
22	chr4:86699962-86700012	Jurkat	blood:	n/a
23	chr4:86708298-86708348	HRE	kidney:	n/a
24	chr4:86718190-86718240	AoSMC	blood vessel:	n/a
25	chr4:86705640-86705690	HL-60	blood:	n/a
26	chr4:86682649-86682699	HL-60	blood:	n/a
27	chr4:86699705-86699755	A549	lung:	n/a
28	chr4:86682649-86682699	BE2_C	brain:	n/a
29	chr4:86718190-86718240	HCF	heart:	n/a
30	chr4:86718190-86718240	SAEC	small airway:	n/a
31	chr4:86682649-86682699	HCPEpiC	choroid plexus:	n/a
32	chr4:86705640-86705690	Jurkat	blood:	n/a
33	chr4:86718190-86718240	HRCEpiC	kidney:	n/a
34	chr4:86699705-86699755	NT2-D1	testis:	n/a
35	chr4:86699962-86700012	Caco-2	colon:	n/a
36	chr4:86718190-86718240	HL-60	blood:	n/a
37	chr4:86682649-86682699	SK-N-MC	brain:	n/a
38	chr4:86682649-86682699	AG09319	gingival:	n/a
39	chr4:86718190-86718240	AG09309	skin:	n/a
40	chr4:86699962-86700012	NT2-D1	testis:	n/a
41	chr4:86682649-86682699	PrEC	prostate:	n/a
42	chr4:86705640-86705690	SKMC	muscle:	n/a
43	chr4:86718190-86718240	GM19239	blood:	n/a
44	chr4:86699705-86699755	HNPCEpiC	eye:	n/a
45	chr4:86705640-86705690	A549	lung:	n/a
46	chr4:86708298-86708348	HRPEpiC	eye:	n/a
47	chr4:86682649-86682699	HMEC	breast:	n/a
48	chr4:86718190-86718240	HNPCEpiC	eye:	n/a
49	chr4:86705640-86705690	HEK293	kidney:	embryo
50	chr4:86699705-86699755	HRCEpiC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:86709819..86711505-chr4:86721920..86724545,2	MCF-7	breast:
2	chr4:86717573..86718676-chr4:86889897..86890637,3	MCF-7	breast:
3	chr4:86678039..86678782-chr4:86890252..86890768,2	MCF-7	breast:
4	chr4:86709819..86711505-chr4:86721920..86724545,2	MCF-7	breast:
5	chr4:86678145..86678790-chr4:86717860..86718656,2	MCF-7	breast:
6	chr4:86721706..86723573-chr4:86724471..86726951,3	MCF-7	breast:
7	chr4:86728075..86730663-chr4:86957838..86959662,2	MCF-7	breast:
8	chr4:86717783..86718591-chr4:86885186..86885920,6	MCF-7	breast:
9	chr4:86678145..86678790-chr4:86717860..86718656,2	MCF-7	breast:
10	chr4:86717774..86718537-chr4:86886876..86887427,3	MCF-7	breast:
11	chr4:86713042..86715039-chr4:87371799..87373395,2	MCF-7	breast:
12	chr4:86721706..86723573-chr4:86724471..86726951,3	MCF-7	breast:
13	chr4:86669212..86669756-chr4:86677606..86678326,2	MCF-7	breast:
14	chr4:86699451..86703287-chr4:86705841..86708546,3	MCF-7	breast:
15	chr4:86717537..86719169-chr4:86889518..86891294,13	MCF-7	breast:
16	chr4:86717526..86718413-chr4:86964881..86965596,2	MCF-7	breast:
17	chr4:86717637..86718454-chr4:86964866..86965718,3	MCF-7	breast:
18	chr4:86717884..86718437-chr4:86885535..86886084,2	MCF-7	breast:

No data

Variant related genes	Relation type
ARHGAP24	TF binding region
ARHGAP24	CpG island
ENSG00000138639	chromatin interactions

Extended variants
information (count: 2149 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2149 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4693735	chr4:86677107-86677108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375987195	chr4:86677133-86677134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537252487	chr4:86677142-86677143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559539736	chr4:86677198-86677199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558650884	chr4:86677234-86677235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112486882	chr4:86677289-86677290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540794758	chr4:86677304-86677305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192573983	chr4:86677345-86677346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs386676895	chr4:86677362-86677363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200950869	chr4:86677363-86677364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368983340	chr4:86677365-86677366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200470412	chr4:86677366-86677367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201435233	chr4:86677367-86677368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138218235	chr4:86677411-86677412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73833238	chr4:86677477-86677478	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs563650446	chr4:86677486-86677487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368617040	chr4:86677565-86677566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372077052	chr4:86677590-86677591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149527725	chr4:86677633-86677634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552378200	chr4:86677664-86677665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143660553	chr4:86677701-86677702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs559412709	chr4:86677707-86677708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376503364	chr4:86677709-86677710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551408190	chr4:86677729-86677730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200665851	chr4:86677742-86677743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113209604	chr4:86677765-86677766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571027432	chr4:86677812-86677813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114014161	chr4:86677914-86677915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540138935	chr4:86678017-86678018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535483503	chr4:86678019-86678020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs148074088	chr4:86678105-86678106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527529558	chr4:86678154-86678155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552065002	chr4:86678219-86678220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564442476	chr4:86678226-86678227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537215552	chr4:86678236-86678237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141916498	chr4:86678265-86678266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577141171	chr4:86678315-86678316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185556332	chr4:86678343-86678344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552837642	chr4:86678356-86678357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs62315340	chr4:86678364-86678365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567221846	chr4:86678366-86678367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs66840348	chr4:86678384-86678385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62315341	chr4:86678385-86678386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369021721	chr4:86678456-86678457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550238971	chr4:86678477-86678478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372562408	chr4:86678485-86678486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs386676896	chr4:86678524-86678525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6819529	chr4:86678526-86678527	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs564331840	chr4:86678534-86678535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528727271	chr4:86678543-86678544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86663400-86699800	Weak transcription	Fetal Muscle Trunk	muscle
2	chr4:86666000-86682400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr4:86667600-86678000	Weak transcription	Stomach Mucosa	stomach
4	chr4:86668000-86677800	Weak transcription	Right Atrium	heart
5	chr4:86670400-86683600	Weak transcription	HSMMtube	muscle
6	chr4:86670600-86680400	Weak transcription	HUVEC	blood vessel
7	chr4:86671600-86681800	Weak transcription	Fetal Muscle Leg	muscle
8	chr4:86673000-86679800	Weak transcription	Primary B cells from cord blood	blood
9	chr4:86673400-86680600	Weak transcription	NHDF-Ad	bronchial
10	chr4:86673400-86682400	Weak transcription	Spleen	Spleen
11	chr4:86673400-86683400	Weak transcription	HSMM	muscle
12	chr4:86673600-86677600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:86673600-86681800	Weak transcription	Right Ventricle	heart
14	chr4:86673600-86683800	Weak transcription	Left Ventricle	heart
15	chr4:86674000-86679000	Weak transcription	Primary B cells from peripheral blood	blood
16	chr4:86674800-86677600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:86674800-86685400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:86676200-86680600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr4:86676200-86683000	Weak transcription	Colon Smooth Muscle	Colon
20	chr4:86676400-86677800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:86676400-86677800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:86676400-86682800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr4:86676600-86680400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr4:86676600-86681800	Weak transcription	Adipose Nuclei	Adipose
25	chr4:86676600-86681800	Weak transcription	Pancreas	Pancrea
26	chr4:86676600-86682800	Weak transcription	Brain Anterior Caudate	brain
27	chr4:86676800-86682200	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr4:86676800-86697800	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr4:86677600-86678200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:86677600-86678200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:86677800-86678200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:86677800-86678200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr4:86677800-86678200	Enhancers	Osteobl	bone
34	chr4:86677800-86678400	Enhancers	Gastric	stomach
35	chr4:86677800-86678400	Enhancers	Right Atrium	heart
36	chr4:86678200-86680400	Weak transcription	Osteobl	bone
37	chr4:86678200-86680600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:86678200-86680600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr4:86678200-86682800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:86678200-86685200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr4:86678400-86682800	Weak transcription	Right Atrium	heart
42	chr4:86679000-86684600	Strong transcription	Primary B cells from peripheral blood	blood
43	chr4:86679400-86679600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:86679600-86679800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr4:86679800-86680000	Strong transcription	Primary B cells from cord blood	blood
46	chr4:86679800-86681000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr4:86680000-86680600	Weak transcription	Primary B cells from cord blood	blood
48	chr4:86680000-86682000	Weak transcription	Fetal Brain Male	brain
49	chr4:86680400-86680600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr4:86680400-86682400	Enhancers	Fetal Lung	lung

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