Variant report

Variant	nsv999482
Chromosome Location	chr4:20546216-20563747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:20546356-20546601	HepG2	liver:	n/a	n/a
2	CTCF	chr4:20546380-20546530	GM12865	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
3	CTCF	chr4:20546303-20546629	HepG2	liver:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
4	CTCF	chr4:20546406-20546578	GM12878	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
5	CTCF	chr4:20546480-20546630	HFF	foreskin:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
6	CTCF	chr4:20546797-20546826	Gliobla	brain:	n/a	n/a
7	CTCF	chr4:20546391-20546577	A549	lung:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
8	CTCF	chr4:20546391-20546598	LNCaP	prostate:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
9	CTCF	chr4:20546440-20546590	NB4	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
10	CTCF	chr4:20546380-20546530	HVMF	connective:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
11	CTCF	chr4:20546400-20546550	HEK293	kidney:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
12	CTCF	chr4:20546440-20546590	HMF	breast:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
13	CTCF	chr4:20546420-20546570	HCM	heart:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
14	CTCF	chr4:20546400-20546550	GM12873	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
15	CTCF	chr4:20546260-20546594	T-47D	breast:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
16	CTCF	chr4:20546400-20546550	AoAF	blood vessel:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
17	CTCF	chr4:20546560-20546710	WI-38	lung:	n/a	n/a
18	CTCF	chr4:20546336-20546628	H1-hESC	embryonic stem cell:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
19	CTCF	chr4:20546420-20546570	HPAF	blood vessel:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
20	CTCF	chr4:20546134-20546889	SK-N-SH	brain:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
21	CTCF	chr4:20546560-20546710	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr4:20546422-20546589	Lung_OC	lung:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
23	CTCF	chr4:20546440-20546590	SAEC	small airway:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
24	CTCF	chr4:20546420-20546570	AG09309	skin:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
25	CTCF	chr4:20546440-20546590	HCFaa	heart:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
26	CTCF	chr4:20546440-20546590	AG04450	lung:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
27	CTCF	chr4:20546740-20546890	AG10803	skin:	n/a	n/a
28	CTCF	chr4:20546394-20546604	Kidney_OC	kidney:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
29	CTCF	chr4:20546380-20546539	A549	lung:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
30	CTCF	chr4:20546363-20546629	Medullo	brain:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
31	CTCF	chr4:20546400-20546550	K562	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
32	CTCF	chr4:20546351-20546803	A549	lung:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
33	CTCF	chr4:20546380-20546530	HBMEC	blood vessel:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
34	CTCF	chr4:20546304-20546667	GM12878	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
35	CTCF	chr4:20546360-20546510	GM12864	blood:	n/a	chr4:20546488-20546509 chr4:20546498-20546506
36	CTCF	chr4:20546460-20546610	GM12874	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
37	CTCF	chr4:20546320-20546470	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr4:20546420-20546570	GM12872	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
39	CTCF	chr4:20546380-20546530	GM12878	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
40	CTCF	chr4:20546420-20546570	GM12875	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
41	CTCF	chr4:20546780-20546868	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr4:20546420-20546570	HepG2	liver:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
43	CTCF	chr4:20546480-20546630	K562	blood:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
44	CTCF	chr4:20546796-20546866	GM19238	blood:	n/a	n/a
45	CTCF	chr4:20546480-20546630	NHLF	lung:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
46	CTCF	chr4:20546360-20546510	A549	lung:	n/a	chr4:20546488-20546509 chr4:20546498-20546506
47	CTCF	chr4:20546420-20546570	BJ	skin:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
48	CTCF	chr4:20546440-20546590	HEK293	kidney:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
49	CTCF	chr4:20546387-20546642	MCF-7	breast:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506
50	CTCF	chr4:20546380-20546530	Hela-S3	cervix:	n/a	chr4:20546488-20546509 chr4:20546493-20546511 chr4:20546498-20546506

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:20558003-20558053	HIPEpiC	eye:	n/a
2	chr4:20558003-20558053	HCM	heart:	n/a
3	chr4:20558003-20558053	HMEC	breast:	n/a
4	chr4:20558003-20558053	U87	brain:	n/a
5	chr4:20558003-20558053	HepG2	liver:	n/a
6	chr4:20558003-20558053	HL-60	blood:	n/a
7	chr4:20558003-20558053	H1-hESC	embryonic stem cell:	embryo
8	chr4:20558003-20558053	SKMC	muscle:	n/a
9	chr4:20558003-20558053	NH-A	brain:	n/a
10	chr4:20558003-20558053	GM12892	blood:	n/a
11	chr4:20558003-20558053	HCF	heart:	n/a
12	chr4:20558003-20558053	ProgFib	skin:	n/a
13	chr4:20558003-20558053	NHBE	bronchial:	n/a
14	chr4:20558003-20558053	HRE	kidney:	n/a
15	chr4:20558003-20558053	NT2-D1	testis:	n/a
16	chr4:20558003-20558053	MCF-7	breast:	n/a
17	chr4:20558003-20558053	AoSMC	blood vessel:	n/a
18	chr4:20558003-20558053	HCT-116	colon:	n/a
19	chr4:20558003-20558053	RPTEC	kidney:	n/a
20	chr4:20558003-20558053	Hepatocyte	liver:	n/a
21	chr4:20558003-20558053	AG10803	skin:	n/a
22	chr4:20558003-20558053	HEEpiC	esophagus:	n/a
23	chr4:20558003-20558053	MCF10A-Er-Src	breast:	n/a
24	chr4:20558003-20558053	NHDF-neo	bronchial:	n/a
25	chr4:20558003-20558053	A549	lung:	n/a
26	chr4:20558003-20558053	AG04450	lung:	fetal
27	chr4:20558003-20558053	T-47D	breast:	n/a
28	chr4:20558003-20558053	SK-N-SH_RA	brain:	n/a
29	chr4:20558003-20558053	HRCEpiC	kidney:	n/a
30	chr4:20558003-20558053	HCPEpiC	choroid plexus:	n/a
31	chr4:20558003-20558053	PANC-1	pancreas:	n/a
32	chr4:20558003-20558053	Jurkat	blood:	n/a
33	chr4:20558003-20558053	AG04449	skin:	fetal
34	chr4:20558003-20558053	PrEC	prostate:	n/a
35	chr4:20558003-20558053	SK-N-SH	brain:	n/a
36	chr4:20558003-20558053	HUVEC	blood vessel:	n/a
37	chr4:20558003-20558053	NB4	blood:	n/a
38	chr4:20558003-20558053	GM12878	blood:	n/a
39	chr4:20558003-20558053	IMR90	lung:	fetal
40	chr4:20558003-20558053	ECC-1	luminal epithelium:	n/a
41	chr4:20558003-20558053	SK-N-MC	brain:	n/a
42	chr4:20558003-20558053	ovcar-3	ovarian:	n/a
43	chr4:20558003-20558053	GM06990	blood:	n/a
44	chr4:20558003-20558053	SAEC	small airway:	n/a
45	chr4:20558003-20558053	Hela-S3	cervix:	n/a
46	chr4:20558003-20558053	GM12891	blood:	n/a
47	chr4:20558003-20558053	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:20558003-20558053	Caco-2	colon:	n/a
49	chr4:20558003-20558053	AG09309	skin:	n/a
50	chr4:20558003-20558053	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20423426..20426001-chr4:20546337..20549229,2	MCF-7	breast:
2	chr4:20420248..20420749-chr4:20545895..20546523,2	MCF-7	breast:
3	chr4:20555967..20557515-chr4:20560187..20562969,2	K562	blood:
4	chr4:20420286..20420873-chr4:20546445..20547011,2	MCF-7	breast:
5	chr4:20555229..20557515-chr4:20560187..20562423,2	K562	blood:
6	chr4:20423666..20425699-chr4:20545912..20547306,15	MCF-7	breast:
7	chr4:20423772..20424684-chr4:20546066..20546731,4	MCF-7	breast:
8	chr4:20430173..20430714-chr4:20546050..20546559,2	MCF-7	breast:
9	chr4:20301094..20301849-chr4:20546151..20546964,2	MCF-7	breast:
10	chr4:20555967..20557515-chr4:20560187..20562969,2	K562	blood:
11	chr4:20396516..20397430-chr4:20546057..20546973,2	K562	blood:
12	chr4:20423854..20424427-chr4:20546379..20546991,2	K562	blood:

Variant related genes	Relation type
SLIT2	TF binding region
SLIT2	CpG island
ENSG00000145147	chromatin interactions

Extended variants
information (count: 681 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:681 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149274362	chr4:20546242-20546243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73110512	chr4:20546247-20546248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs376355009	chr4:20546297-20546298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180929264	chr4:20546299-20546300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs35153630	chr4:20546315-20546316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554172405	chr4:20546388-20546389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573032936	chr4:20546459-20546460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34487429	chr4:20546465-20546466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs184005451	chr4:20546556-20546557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558465140	chr4:20546656-20546657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576931036	chr4:20546685-20546686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368680864	chr4:20546701-20546702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544424163	chr4:20546708-20546709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144532229	chr4:20546732-20546733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs12501533	chr4:20546776-20546777	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs77586665	chr4:20546789-20546790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs188678977	chr4:20546854-20546855	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527973615	chr4:20547031-20547032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148449282	chr4:20547035-20547036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181418140	chr4:20547042-20547043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537738433	chr4:20547050-20547051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186707313	chr4:20547059-20547060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10541468	chr4:20547082-20547083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72209009	chr4:20547089-20547090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3836701	chr4:20547100-20547101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549984451	chr4:20547150-20547151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568201145	chr4:20547177-20547178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535581830	chr4:20547212-20547213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547472304	chr4:20547274-20547275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12505707	chr4:20547287-20547288	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs560728439	chr4:20547346-20547347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192010097	chr4:20547380-20547381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182016467	chr4:20547384-20547385	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144113629	chr4:20547413-20547414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577234773	chr4:20547453-20547454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577762853	chr4:20547465-20547466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538008157	chr4:20547466-20547467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556424377	chr4:20547473-20547474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375326031	chr4:20547477-20547478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187569664	chr4:20547480-20547481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190657699	chr4:20547514-20547515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs12501787	chr4:20547532-20547533	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs115696681	chr4:20547557-20547558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12501870	chr4:20547578-20547579	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs368960178	chr4:20547596-20547597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549941563	chr4:20547616-20547617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373582486	chr4:20547628-20547629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182241274	chr4:20547641-20547642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201370366	chr4:20547671-20547672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140806587	chr4:20547672-20547673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:132 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20492000-20599800	Weak transcription	Aorta	Aorta
2	chr4:20511800-20576200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:20519400-20571000	Weak transcription	Adipose Nuclei	Adipose
4	chr4:20524200-20555200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr4:20525200-20555400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr4:20530000-20546400	Weak transcription	Pancreas	Pancrea
7	chr4:20530400-20555400	Weak transcription	NHEK	skin
8	chr4:20533000-20578000	Weak transcription	NHLF	lung
9	chr4:20533800-20576200	Weak transcription	Left Ventricle	heart
10	chr4:20534600-20552800	Weak transcription	Brain Anterior Caudate	brain
11	chr4:20534800-20576400	Weak transcription	Fetal Brain Male	brain
12	chr4:20535800-20593600	Weak transcription	Fetal Kidney	kidney
13	chr4:20536000-20548600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:20536000-20552400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr4:20536000-20554800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr4:20536000-20555200	Weak transcription	Fetal Muscle Trunk	muscle
17	chr4:20536600-20572200	Weak transcription	Placenta	Placenta
18	chr4:20536800-20618600	Weak transcription	Spleen	Spleen
19	chr4:20537800-20552600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr4:20537800-20552600	Weak transcription	Colon Smooth Muscle	Colon
21	chr4:20537800-20552800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr4:20538000-20553200	Weak transcription	Fetal Stomach	stomach
23	chr4:20539000-20552800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:20541200-20546800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:20541200-20552800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr4:20543600-20549600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:20543600-20549800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr4:20545000-20546800	Weak transcription	NHDF-Ad	bronchial
29	chr4:20545000-20547400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr4:20545000-20549800	Weak transcription	Osteobl	bone
31	chr4:20545000-20552600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:20545200-20546800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr4:20545200-20546800	Weak transcription	Fetal Lung	lung
34	chr4:20546800-20547800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr4:20546800-20548000	Strong transcription	NHDF-Ad	bronchial
36	chr4:20546800-20550000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:20546800-20550600	Strong transcription	Fetal Lung	lung
38	chr4:20547000-20576000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr4:20547400-20550800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:20547800-20549800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:20548000-20550000	Weak transcription	NHDF-Ad	bronchial
42	chr4:20548600-20549200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:20548800-20549200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:20549200-20568800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:20549600-20550600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:20549800-20550600	Strong transcription	Placenta Amnion	Placenta Amnion
47	chr4:20549800-20550600	Strong transcription	Osteobl	bone
48	chr4:20549800-20550800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:20550000-20550400	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:20550000-20561400	Strong transcription	NHDF-Ad	bronchial

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