Variant report

Variant	nsv878733
Chromosome Location	chr4:19335464-19928602
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	chr4:19573255-19573311	K562	blood:	n/a	n/a
2	BACH1	chr4:19475319-19475456	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:19415486-19415682	K562	blood:	n/a	n/a
4	BACH1	chr4:19417217-19417398	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr4:19431358-19431619	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr4:19431390-19431625	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr4:19488093-19488406	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr4:19740513-19741195	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr4:19777588-19778204	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr4:19740526-19741097	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:19777467-19778284	HCT-116	colon:	n/a	n/a
12	CBX3	chr4:19740518-19741116	HCT-116	colon:	n/a	n/a
13	CCNT2	chr4:19725134-19725584	K562	blood:	n/a	n/a
14	CEBPB	chr4:19487925-19488399	ECC-1	luminal epithelium:	n/a	chr4:19488095-19488108
15	CEBPB	chr4:19916304-19916655	IMR90	lung:	n/a	chr4:19916483-19916494 chr4:19916484-19916495
16	CEBPB	chr4:19488001-19488411	ECC-1	luminal epithelium:	n/a	chr4:19488095-19488108
17	CEBPB	chr4:19581742-19582149	ECC-1	luminal epithelium:	n/a	chr4:19581869-19581878 chr4:19581869-19581878 chr4:19581868-19581879 chr4:19581869-19581878 chr4:19581867-19581880 chr4:19581869-19581878 chr4:19581867-19581878 chr4:19581867-19581880 chr4:19581867-19581878
18	CEBPB	chr4:19691121-19691499	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr4:19581694-19582062	IMR90	lung:	n/a	chr4:19581869-19581878 chr4:19581869-19581878 chr4:19581868-19581879 chr4:19581869-19581878 chr4:19581867-19581880 chr4:19581869-19581878 chr4:19581867-19581878 chr4:19581867-19581880 chr4:19581867-19581878
20	CEBPB	chr4:19591657-19591874	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:19408909-19409186	IMR90	lung:	n/a	chr4:19409041-19409052
22	CEBPB	chr4:19382661-19383037	Hela-S3	cervix:	n/a	chr4:19382824-19382837
23	CEBPB	chr4:19758300-19758642	IMR90	lung:	n/a	chr4:19758461-19758472 chr4:19758479-19758490
24	CEBPB	chr4:19807640-19807945	IMR90	lung:	n/a	chr4:19807795-19807806 chr4:19807861-19807873 chr4:19807795-19807808
25	CEBPB	chr4:19758302-19758602	ECC-1	luminal epithelium:	n/a	chr4:19758461-19758472 chr4:19758479-19758490
26	CEBPB	chr4:19704095-19704358	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:19750188-19750298	K562	blood:	n/a	chr4:19750269-19750280
28	CEBPB	chr4:19384647-19384913	A549	lung:	n/a	chr4:19384742-19384753
29	CEBPB	chr4:19510097-19510450	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:19758379-19758600	A549	lung:	n/a	chr4:19758461-19758472 chr4:19758479-19758490
31	CEBPB	chr4:19625446-19625847	Hela-S3	cervix:	n/a	chr4:19625589-19625602
32	CEBPB	chr4:19581725-19582056	HepG2	liver:	n/a	chr4:19581869-19581878 chr4:19581869-19581878 chr4:19581868-19581879 chr4:19581869-19581878 chr4:19581867-19581880 chr4:19581869-19581878 chr4:19581867-19581878 chr4:19581867-19581880 chr4:19581867-19581878
33	CEBPB	chr4:19916399-19916665	A549	lung:	n/a	chr4:19916483-19916494 chr4:19916484-19916495
34	CEBPB	chr4:19359574-19360172	HCT-116	colon:	n/a	chr4:19359723-19359734
35	CEBPB	chr4:19896103-19896389	HepG2	liver:	n/a	chr4:19896244-19896255
36	CEBPB	chr4:19750041-19750472	IMR90	lung:	n/a	chr4:19750269-19750280
37	CEBPB	chr4:19843180-19843400	A549	lung:	n/a	chr4:19843221-19843232
38	CEBPB	chr4:19777603-19778293	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:19740579-19741074	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr4:19581711-19581983	H1-hESC	embryonic stem cell:	n/a	chr4:19581869-19581878 chr4:19581869-19581878 chr4:19581868-19581879 chr4:19581869-19581878 chr4:19581867-19581880 chr4:19581869-19581878 chr4:19581867-19581878 chr4:19581867-19581880 chr4:19581867-19581878
41	CEBPB	chr4:19636971-19637217	HepG2	liver:	n/a	chr4:19637088-19637099
42	CEBPB	chr4:19625425-19625800	IMR90	lung:	n/a	chr4:19625589-19625602
43	CEBPB	chr4:19808756-19809489	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:19680301-19680659	IMR90	lung:	n/a	n/a
45	CEBPB	chr4:19808858-19809497	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:19382365-19383114	IMR90	lung:	n/a	chr4:19382824-19382837
47	CEBPB	chr4:19757638-19757900	IMR90	lung:	n/a	chr4:19757716-19757727 chr4:19757718-19757729 chr4:19757716-19757729 chr4:19757748-19757759 chr4:19757746-19757763 chr4:19757747-19757760 chr4:19757716-19757729 chr4:19757718-19757729
48	CEBPB	chr4:19581650-19582075	ECC-1	luminal epithelium:	n/a	chr4:19581869-19581878 chr4:19581869-19581878 chr4:19581868-19581879 chr4:19581869-19581878 chr4:19581867-19581880 chr4:19581869-19581878 chr4:19581867-19581878 chr4:19581867-19581880 chr4:19581867-19581878
49	CEBPB	chr4:19758310-19758636	HepG2	liver:	n/a	chr4:19758461-19758472 chr4:19758479-19758490
50	CEBPB	chr4:19885544-19885857	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:19457049-19457099	Hela-S3	cervix:	n/a
2	chr4:19457049-19457099	Hela-S3	cervix:	n/a
3	chr4:19457040-19457090	MCF-7	breast:	n/a
4	chr4:19457163-19457213	AG10803	skin:	n/a
5	chr4:19750829-19750879	NHBE	bronchial:	n/a
6	chr4:19740944-19740994	HCPEpiC	choroid plexus:	n/a
7	chr4:19750829-19750879	MCF10A-Er-Src	breast:	n/a
8	chr4:19457040-19457090	GM12878	blood:	n/a
9	chr4:19457120-19457170	NHBE	bronchial:	n/a
10	chr4:19750829-19750879	SK-N-SH	brain:	n/a
11	chr4:19777808-19777858	U87	brain:	n/a
12	chr4:19457040-19457090	GM12891	blood:	n/a
13	chr4:19457120-19457170	HRPEpiC	eye:	n/a
14	chr4:19750829-19750879	H1-hESC	embryonic stem cell:	embryo
15	chr4:19740944-19740994	GM19239	blood:	n/a
16	chr4:19750829-19750879	AG04450	lung:	fetal
17	chr4:19750829-19750879	AoSMC	blood vessel:	n/a
18	chr4:19457163-19457213	RPTEC	kidney:	n/a
19	chr4:19457120-19457170	Hepatocyte	liver:	n/a
20	chr4:19777808-19777858	GM12892	blood:	n/a
21	chr4:19750829-19750879	GM12891	blood:	n/a
22	chr4:19750829-19750879	GM06990	blood:	n/a
23	chr4:19750829-19750879	HCPEpiC	choroid plexus:	n/a
24	chr4:19457163-19457213	HCF	heart:	n/a
25	chr4:19750829-19750879	Hepatocyte	liver:	n/a
26	chr4:19740944-19740994	CMK	blood:	n/a
27	chr4:19740944-19740994	BJ	skin:	n/a
28	chr4:19457040-19457090	NH-A	brain:	n/a
29	chr4:19777808-19777858	SK-N-MC	brain:	n/a
30	chr4:19457120-19457170	RPTEC	kidney:	n/a
31	chr4:19740944-19740994	AG10803	skin:	n/a
32	chr4:19457040-19457090	BE2_C	brain:	n/a
33	chr4:19457040-19457090	BJ	skin:	n/a
34	chr4:19750829-19750879	HCM	heart:	n/a
35	chr4:19740944-19740994	RPTEC	kidney:	n/a
36	chr4:19457040-19457090	SK-N-MC	brain:	n/a
37	chr4:19457120-19457170	AG10803	skin:	n/a
38	chr4:19457163-19457213	U87	brain:	n/a
39	chr4:19740944-19740994	HMEC	breast:	n/a
40	chr4:19457040-19457090	RPTEC	kidney:	n/a
41	chr4:19777808-19777858	Hepatocyte	liver:	n/a
42	chr4:19457049-19457099	HCF	heart:	n/a
43	chr4:19777808-19777858	HL-60	blood:	n/a
44	chr4:19750829-19750879	K562	blood:	n/a
45	chr4:19750829-19750879	AG04449	skin:	fetal
46	chr4:19777808-19777858	NHDF-neo	bronchial:	n/a
47	chr4:19750829-19750879	SAEC	small airway:	n/a
48	chr4:19457120-19457170	BE2_C	brain:	n/a
49	chr4:19750829-19750879	PrEC	prostate:	n/a
50	chr4:19457040-19457090	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:19727412..19729321-chr4:19735954..19738022,2	MCF-7	breast:
2	chr4:19559004..19561112-chr4:19562245..19563790,2	MCF-7	breast:
3	chr4:19727412..19729321-chr4:19735954..19738022,2	MCF-7	breast:
4	chr4:19660234..19663712-chr4:19666712..19669075,3	K562	blood:
5	chr4:19442481..19444485-chr4:19446787..19449447,2	K562	blood:
6	chr4:19747370..19749528-chr4:19753933..19756886,2	K562	blood:
7	chr4:19788930..19791158-chr4:19794175..19796183,2	MCF-7	breast:
8	chr4:19788930..19791158-chr4:19794175..19796183,2	MCF-7	breast:
9	chr4:19442481..19444485-chr4:19446787..19449447,2	K562	blood:
10	chr4:19583145..19583681-chr4:62195548..62196296,2	MCF-7	breast:
11	chr4:19660234..19663712-chr4:19666712..19669075,3	K562	blood:
12	chr4:19835706..19836351-chr5:9383849..9384559,2	MCF-7	breast:
13	chr4:19258834..19261386-chr4:19628228..19629933,2	K562	blood:
14	chr4:19559004..19561112-chr4:19562245..19563790,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNIP4-1	chr4:19748802-19748941	XLOC_003902
2	lnc-SLIT2-1	chr4:19457059-19457275	ENSG00000248515.1
3	lnc-SLIT2-1	chr4:19910835-19911315	ENSG00000248515.1
4	lnc-KCNIP4-1	chr4:19756116-19756214	XLOC_003902
5	lnc-SLIT2-1	chr4:19535171-19535241	ENSG00000248515.1
6	lnc-SLIT2-1	chr4:19857899-19858018	ENSG00000248515.1
7	lnc-LCORL-2	chr4:19458269-19458617	ENSG00000248238

Variant related genes	Relation type
ENSG00000248238	TF binding region
ENSG00000249441	TF binding region
ENSG00000248515	TF binding region
ENSG00000241612	TF binding region
ENSG00000248238	CpG island
ENSG00000249441	CpG island
ENSG00000248515	CpG island
ENSG00000241612	CpG island
ENSG00000249441	chromatin interactions
FCHSD2	miRNA target sites
AKT3	miRNA target sites

Extended variants
information (count: 9322 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:9322 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563085395	chr4:19350225-19350226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554199207	chr4:19350238-19350239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113115002	chr4:19350253-19350254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546181441	chr4:19350274-19350275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143147165	chr4:19350343-19350344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs180690315	chr4:19350354-19350355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543975585	chr4:19350382-19350383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs5856504	chr4:19350390-19350391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs397822673	chr4:19350400-19350401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11943058	chr4:19350406-19350407	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs147505466	chr4:19350434-19350435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541486303	chr4:19350452-19350453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564248631	chr4:19350476-19350477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532871906	chr4:19350488-19350489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527253785	chr4:19350558-19350559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73800857	chr4:19350693-19350694	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs28550577	chr4:19350714-19350715	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs79437739	chr4:19350758-19350759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369909396	chr4:19350778-19350779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543777106	chr4:19350787-19350788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1490878	chr4:19350814-19350815	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs1490879	chr4:19350875-19350876	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs548821274	chr4:19350895-19350896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186450821	chr4:19350920-19350921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189293402	chr4:19350940-19350941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547862690	chr4:19350947-19350948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs1490880	chr4:19350950-19350951	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs145627169	chr4:19350972-19350973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181862539	chr4:19351004-19351005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557657607	chr4:19351037-19351038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186881962	chr4:19351041-19351042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12643303	chr4:19351058-19351059	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555553394	chr4:19351104-19351105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573851080	chr4:19351167-19351168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541548167	chr4:19351252-19351253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144397383	chr4:19351265-19351266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77085690	chr4:19351289-19351290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115470034	chr4:19351300-19351301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564267629	chr4:19351329-19351330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531624561	chr4:19351479-19351480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550059250	chr4:19351482-19351483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116070486	chr4:19351505-19351506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370454282	chr4:19351510-19351511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529070771	chr4:19351520-19351521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547947671	chr4:19351531-19351532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs566144105	chr4:19351587-19351588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539496873	chr4:19351627-19351628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148390075	chr4:19351649-19351650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574044782	chr4:19351672-19351673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191470743	chr4:19351708-19351709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	16774939	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19350200-19351200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:19351000-19351400	Enhancers	NHEK	skin
3	chr4:19351000-19351600	Enhancers	HMEC	breast
4	chr4:19351200-19351400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:19351400-19367400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:19358000-19358400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:19359000-19360600	Enhancers	NHEK	skin
8	chr4:19359400-19360600	Enhancers	HMEC	breast
9	chr4:19360000-19360600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:19360000-19360600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:19361200-19361800	Enhancers	Brain Substantia Nigra	brain
12	chr4:19361400-19361800	Enhancers	Brain Hippocampus Middle	brain
13	chr4:19367400-19367600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:19367400-19368000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:19367800-19369200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:19369200-19376800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:19376800-19377400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:19376800-19377800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:19376800-19377800	Enhancers	NHDF-Ad	bronchial
20	chr4:19377000-19377400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr4:19377000-19377400	Enhancers	NHLF	lung
22	chr4:19377000-19377600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:19377200-19377800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:19377400-19381800	Weak transcription	NHLF	lung
25	chr4:19377400-19382200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr4:19377800-19382000	Weak transcription	NHDF-Ad	bronchial
27	chr4:19377800-19382400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr4:19377800-19383000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr4:19380800-19383800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr4:19381200-19383800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:19381800-19383400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr4:19381800-19383400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:19381800-19383400	Enhancers	HMEC	breast
34	chr4:19381800-19383800	Enhancers	NHLF	lung
35	chr4:19382000-19383400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr4:19382000-19383400	Enhancers	NHDF-Ad	bronchial
37	chr4:19382000-19383400	Enhancers	Osteobl	bone
38	chr4:19382000-19383600	Enhancers	NHEK	skin
39	chr4:19382200-19383400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr4:19382400-19383200	Enhancers	NH-A	brain
41	chr4:19382400-19385600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:19383000-19383800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr4:19383000-19383800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr4:19383400-19384400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr4:19383400-19384400	Weak transcription	NHDF-Ad	bronchial
46	chr4:19383400-19384600	Weak transcription	Osteobl	bone
47	chr4:19383400-19388400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr4:19383400-19388400	Weak transcription	HMEC	breast
49	chr4:19383800-19384600	Weak transcription	NHLF	lung
50	chr4:19383800-19387600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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