Variant report

Variant	nsv529290
Chromosome Location	chr4:19658583-20173839
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	BACH1	chr4:19987083-19987100	K562	blood:	n/a	n/a
2	BATF	chr4:20052526-20052762	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:20017561-20017815	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:20052554-20052704	GM12878	blood:	n/a	n/a
5	BRCA1	chr4:19777588-19778204	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr4:19740513-19741195	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr4:20030228-20030821	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr4:19740526-19741097	HCT-116	colon:	n/a	n/a
9	CBX3	chr4:19740518-19741116	HCT-116	colon:	n/a	n/a
10	CBX3	chr4:19777467-19778284	HCT-116	colon:	n/a	n/a
11	CCNT2	chr4:20070197-20070341	K562	blood:	n/a	n/a
12	CCNT2	chr4:19725134-19725584	K562	blood:	n/a	n/a
13	CEBPB	chr4:19750041-19750472	IMR90	lung:	n/a	chr4:19750269-19750280
14	CEBPB	chr4:19980786-19981132	HepG2	liver:	n/a	chr4:19980961-19980972
15	CEBPB	chr4:19758300-19758642	IMR90	lung:	n/a	chr4:19758461-19758472 chr4:19758479-19758490
16	CEBPB	chr4:19980806-19981047	A549	lung:	n/a	chr4:19980961-19980972
17	CEBPB	chr4:20088542-20088852	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:20128178-20128935	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:19808756-19809489	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:19758303-19758599	H1-hESC	embryonic stem cell:	n/a	chr4:19758461-19758472 chr4:19758479-19758490
21	CEBPB	chr4:19896074-19896300	A549	lung:	n/a	chr4:19896244-19896255
22	CEBPB	chr4:20021650-20022311	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:19813832-19814087	IMR90	lung:	n/a	chr4:19813957-19813968 chr4:19813957-19813968 chr4:19813899-19813912
24	CEBPB	chr4:20088609-20088850	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:19777549-19778126	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr4:19933278-19933565	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:19740579-19741074	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr4:20166724-20166989	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:19916304-19916655	IMR90	lung:	n/a	chr4:19916483-19916494 chr4:19916484-19916495
30	CEBPB	chr4:19885544-19885857	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:19704095-19704358	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr4:19750109-19750429	A549	lung:	n/a	chr4:19750269-19750280
33	CEBPB	chr4:20138879-20139168	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:19757622-19757822	A549	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
35	CEBPB	chr4:19736659-19737015	IMR90	lung:	n/a	chr4:19736669-19736682 chr4:19736840-19736857 chr4:19736669-19736682 chr4:19736671-19736682
36	CEBPB	chr4:20098582-20098913	HepG2	liver:	n/a	chr4:20098734-20098745 chr4:20098747-20098758 chr4:20098736-20098747
37	CEBPB	chr4:19916328-19916658	HepG2	liver:	n/a	chr4:19916483-19916494 chr4:19916484-19916495
38	CEBPB	chr4:19750145-19750408	HepG2	liver:	n/a	chr4:19750269-19750280
39	CEBPB	chr4:19980803-19981133	IMR90	lung:	n/a	chr4:19980961-19980972
40	CEBPB	chr4:20046045-20046765	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr4:19758262-19758879	Hela-S3	cervix:	n/a	chr4:19758461-19758472 chr4:19758479-19758490
42	CEBPB	chr4:19736634-19737386	Hela-S3	cervix:	n/a	chr4:19736669-19736682 chr4:19736840-19736857 chr4:19736669-19736682 chr4:19736671-19736682
43	CEBPB	chr4:19948983-19949328	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:19757579-19757872	HepG2	liver:	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
45	CEBPB	chr4:20089137-20089636	HepG2	liver:	n/a	chr4:20089289-20089300 chr4:20089604-20089615 chr4:20089602-20089615 chr4:20089602-20089615 chr4:20089602-20089615 chr4:20089599-20089616 chr4:20089604-20089615
46	CEBPB	chr4:20089123-20089422	H1-hESC	embryonic stem cell:	n/a	chr4:20089289-20089300
47	CEBPB	chr4:19744731-19745101	Hela-S3	cervix:	n/a	chr4:19744911-19744922 chr4:19744909-19744922 chr4:19744919-19744932 chr4:19744919-19744932 chr4:19744911-19744922
48	CEBPB	chr4:19750112-19750408	Hela-S3	cervix:	n/a	chr4:19750269-19750280
49	CEBPB	chr4:19808858-19809497	IMR90	lung:	n/a	n/a
50	CEBPB	chr4:19774970-19775238	HepG2	liver:	n/a	chr4:19775090-19775101

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:19750829-19750879	Hela-S3	cervix:	n/a
2	chr4:20018421-20018471	AG09309	skin:	n/a
3	chr4:20018421-20018471	Hela-S3	cervix:	n/a
4	chr4:19750829-19750879	NH-A	brain:	n/a
5	chr4:19984063-19984113	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:19750829-19750879	AG10803	skin:	n/a
7	chr4:20044588-20044638	PFSK-1	brain:	n/a
8	chr4:20006267-20006317	SAEC	small airway:	n/a
9	chr4:19962859-19962909	GM12891	blood:	n/a
10	chr4:19750829-19750879	IMR90	lung:	fetal
11	chr4:19984063-19984113	PrEC	prostate:	n/a
12	chr4:19962859-19962909	AG04449	skin:	fetal
13	chr4:19777808-19777858	HCPEpiC	choroid plexus:	n/a
14	chr4:19984063-19984113	ECC-1	luminal epithelium:	n/a
15	chr4:19750829-19750879	HMEC	breast:	n/a
16	chr4:19750829-19750879	NB4	blood:	n/a
17	chr4:19740944-19740994	HRE	kidney:	n/a
18	chr4:19750829-19750879	Hepatocyte	liver:	n/a
19	chr4:19740944-19740994	HCF	heart:	n/a
20	chr4:20018421-20018471	HUVEC	blood vessel:	n/a
21	chr4:20006267-20006317	Caco-2	colon:	n/a
22	chr4:19962859-19962909	GM12878	blood:	n/a
23	chr4:19740944-19740994	HCT-116	colon:	n/a
24	chr4:20006267-20006317	AG09319	gingival:	n/a
25	chr4:19777808-19777858	SKMC	muscle:	n/a
26	chr4:20006267-20006317	SK-N-MC	brain:	n/a
27	chr4:19750829-19750879	HEK293	kidney:	embryo
28	chr4:20044588-20044638	HMEC	breast:	n/a
29	chr4:20044588-20044638	PrEC	prostate:	n/a
30	chr4:20018421-20018471	SKMC	muscle:	n/a
31	chr4:20044588-20044638	HCM	heart:	n/a
32	chr4:19777808-19777858	AG04449	skin:	fetal
33	chr4:19777808-19777858	AoSMC	blood vessel:	n/a
34	chr4:19984063-19984113	CMK	blood:	n/a
35	chr4:20044588-20044638	GM12878	blood:	n/a
36	chr4:20006267-20006317	HL-60	blood:	n/a
37	chr4:19740944-19740994	ProgFib	skin:	n/a
38	chr4:20044588-20044638	BE2_C	brain:	n/a
39	chr4:19962859-19962909	K562	blood:	n/a
40	chr4:19962859-19962909	NT2-D1	testis:	n/a
41	chr4:20018421-20018471	GM06990	blood:	n/a
42	chr4:19962859-19962909	HRE	kidney:	n/a
43	chr4:19984063-19984113	AG09309	skin:	n/a
44	chr4:20044588-20044638	HCT-116	colon:	n/a
45	chr4:19962859-19962909	HNPCEpiC	eye:	n/a
46	chr4:19750829-19750879	HIPEpiC	eye:	n/a
47	chr4:19962859-19962909	RPTEC	kidney:	n/a
48	chr4:19984063-19984113	SK-N-SH_RA	brain:	n/a
49	chr4:19750829-19750879	HepG2	liver:	n/a
50	chr4:20044588-20044638	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20087439..20089887-chr4:20127144..20130135,2	K562	blood:
2	chr4:19788930..19791158-chr4:19794175..19796183,2	MCF-7	breast:
3	chr4:20063520..20065653-chr4:20071734..20074613,2	K562	blood:
4	chr4:19727412..19729321-chr4:19735954..19738022,2	MCF-7	breast:
5	chr4:19660234..19663712-chr4:19666712..19669075,3	K562	blood:
6	chr4:19835706..19836351-chr5:9383849..9384559,2	MCF-7	breast:
7	chr4:19727412..19729321-chr4:19735954..19738022,2	MCF-7	breast:
8	chr4:20087439..20089887-chr4:20127144..20130135,2	K562	blood:
9	chr4:19788930..19791158-chr4:19794175..19796183,2	MCF-7	breast:
10	chr4:19660234..19663712-chr4:19666712..19669075,3	K562	blood:
11	chr4:20064153..20065819-chr4:20071734..20073623,2	K562	blood:
12	chr4:20063520..20065653-chr4:20071734..20074613,2	K562	blood:
13	chr4:20025908..20028659-chr4:20253195..20254796,2	MCF-7	breast:
14	chr4:19747370..19749528-chr4:19753933..19756886,2	K562	blood:
15	chr4:20064153..20065819-chr4:20071734..20073623,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNIP4-1	chr4:19748802-19748941	XLOC_003902
2	lnc-KCNIP4-1	chr4:19756116-19756214	XLOC_003902
3	lnc-SLIT2-4	chr4:20004071-20004174	ucscGeneNc_uc003gpt_2
4	lnc-SLIT2-1	chr4:19857899-19858018	ENSG00000248515.1
5	lnc-SLIT2-1	chr4:19910835-19911315	ENSG00000248515.1
6	lnc-SLIT2-4	chr4:20004287-20004380	ucscGeneNc_uc003gpt_2
7	lnc-SLIT2-4	chr4:20005250-20005576	ucscGeneNc_uc003gpt_2
8	lnc-KCNIP4-4	chr4:20039183-20039595	NONHSAT095729
9	lnc-SLIT2-4	chr4:20002917-20002984	ucscGeneNc_uc003gpt_2

Variant related genes	Relation type
ENSG00000250611	TF binding region
ENSG00000249441	TF binding region
ENSG00000241612	TF binding region
ENSG00000250611	CpG island
ENSG00000249441	CpG island
ENSG00000241612	CpG island
ENSG00000249441	chromatin interactions
FCHSD2	miRNA target sites
AKT3	miRNA target sites

Extended variants
information (count: 9268 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:9268 , 50 per page) page: 1 2 3 4 5 6 7 ... 186

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368662877	chr4:19660606-19660607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs36022993	chr4:19660646-19660647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185793258	chr4:19660704-19660705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572097722	chr4:19660711-19660712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192496877	chr4:19660732-19660733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182006585	chr4:19660737-19660738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564646996	chr4:19660786-19660787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573617813	chr4:19660872-19660873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531911110	chr4:19660905-19660906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187105061	chr4:19660922-19660923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs16868667	chr4:19660947-19660948	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs7659519	chr4:19660963-19660964	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs17569535	chr4:19661016-19661017	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs547769479	chr4:19661050-19661051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74902872	chr4:19661095-19661096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539908258	chr4:19661106-19661107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190694984	chr4:19661116-19661117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569838390	chr4:19661147-19661148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35180992	chr4:19661221-19661222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537617327	chr4:19661231-19661232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150163337	chr4:19661234-19661235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567968253	chr4:19661236-19661237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182927489	chr4:19661239-19661240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531582756	chr4:19661266-19661267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138947434	chr4:19661281-19661282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75380996	chr4:19661321-19661322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571972922	chr4:19661420-19661421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75198720	chr4:19661440-19661441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185707372	chr4:19661457-19661458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576213230	chr4:19661464-19661465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190072508	chr4:19661470-19661471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562313104	chr4:19661502-19661503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533399692	chr4:19661542-19661543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs541397240	chr4:19661579-19661580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559679877	chr4:19661644-19661645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs62296884	chr4:19661726-19661727	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs183003363	chr4:19661772-19661773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6848523	chr4:19661776-19661777	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs530915307	chr4:19661842-19661843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547834398	chr4:19661860-19661861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187592728	chr4:19662070-19662071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535716622	chr4:19662075-19662076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73103109	chr4:19662076-19662077	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs565978510	chr4:19662092-19662093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539397367	chr4:19662094-19662095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73103111	chr4:19662160-19662161	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs559195255	chr4:19662173-19662174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368721432	chr4:19664633-19664634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116648863	chr4:19664644-19664645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569202238	chr4:19664700-19664701	Enhancers	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	16774939	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19660600-19661000	Enhancers	Fetal Kidney	kidney
2	chr4:19660800-19661800	Enhancers	HUVEC	blood vessel
3	chr4:19661400-19662200	Enhancers	Dnd41	blood
4	chr4:19664600-19665000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:19664600-19665800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:19668800-19670200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:19676400-19677800	Enhancers	Primary B cells from cord blood	blood
8	chr4:19677000-19677600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:19677000-19677800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:19677000-19677800	Enhancers	Fetal Lung	lung
11	chr4:19677000-19677800	Enhancers	Osteobl	bone
12	chr4:19677000-19678000	Enhancers	Colon Smooth Muscle	Colon
13	chr4:19677200-19677600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:19677200-19677800	Enhancers	Rectal Smooth Muscle	rectum
15	chr4:19677800-19679000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:19677800-19680600	Weak transcription	Osteobl	bone
17	chr4:19679000-19679200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:19679200-19685400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:19680000-19684400	Enhancers	Dnd41	blood
20	chr4:19680400-19681000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr4:19680600-19681000	Enhancers	Osteobl	bone
22	chr4:19680800-19681400	Enhancers	NH-A	brain
23	chr4:19684400-19685200	Enhancers	Fetal Stomach	stomach
24	chr4:19684400-19688000	Weak transcription	Dnd41	blood
25	chr4:19684800-19686600	Enhancers	Fetal Kidney	kidney
26	chr4:19685000-19685400	Enhancers	Colon Smooth Muscle	Colon
27	chr4:19685000-19686600	Enhancers	Rectal Smooth Muscle	rectum
28	chr4:19685200-19685400	Enhancers	Fetal Lung	lung
29	chr4:19685200-19695000	Weak transcription	Fetal Stomach	stomach
30	chr4:19685400-19685600	Flanking Active TSS	Colon Smooth Muscle	Colon
31	chr4:19685400-19686000	Weak transcription	Fetal Lung	lung
32	chr4:19685600-19685800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr4:19685600-19686000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr4:19685600-19686800	Enhancers	Colon Smooth Muscle	Colon
35	chr4:19685800-19686000	Active TSS	NHDF-Ad	bronchial
36	chr4:19685800-19687800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:19686000-19686200	Enhancers	Fetal Lung	lung
38	chr4:19686000-19686200	Flanking Active TSS	NHDF-Ad	bronchial
39	chr4:19686000-19691000	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr4:19686200-19690600	Weak transcription	NHDF-Ad	bronchial
41	chr4:19686200-19695800	Weak transcription	Fetal Lung	lung
42	chr4:19686600-19695800	Weak transcription	Rectal Smooth Muscle	rectum
43	chr4:19687600-19687800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:19687800-19688400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:19687800-19688600	Enhancers	HSMMtube	muscle
46	chr4:19687800-19688800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:19687800-19692000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr4:19688000-19688400	Enhancers	Dnd41	blood
49	chr4:19688400-19694200	Weak transcription	Dnd41	blood
50	chr4:19688600-19691400	Weak transcription	HSMMtube	muscle

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