Variant report

Variant	esv2752044
Chromosome Location	chr4:19788263-20126804
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	chr4:20052554-20052704	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:20017561-20017815	HepG2	liver:	n/a	n/a
5	BRCA1	chr4:20030228-20030821	Hela-S3	cervix:	n/a	n/a
6	CCNT2	chr4:20070197-20070341	K562	blood:	n/a	n/a
7	CEBPB	chr4:19980806-19981047	A549	lung:	n/a	chr4:19980961-19980972
8	CEBPB	chr4:20089123-20089634	IMR90	lung:	n/a	chr4:20089289-20089300 chr4:20089604-20089615 chr4:20089602-20089615 chr4:20089602-20089615 chr4:20089602-20089615 chr4:20089599-20089616 chr4:20089604-20089615
9	CEBPB	chr4:19885544-19885857	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:19984188-19985225	IMR90	lung:	n/a	chr4:19984859-19984871
11	CEBPB	chr4:19948983-19949328	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:19936644-19936844	A549	lung:	n/a	chr4:19936776-19936787
13	CEBPB	chr4:19947699-19948142	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:20018585-20018912	IMR90	lung:	n/a	chr4:20018650-20018663
15	CEBPB	chr4:20021650-20022311	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr4:20047845-20048034	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr4:20089123-20089422	H1-hESC	embryonic stem cell:	n/a	chr4:20089289-20089300
18	CEBPB	chr4:20089277-20089304	K562	blood:	n/a	chr4:20089289-20089300
19	CEBPB	chr4:20098621-20098790	A549	lung:	n/a	chr4:20098734-20098745 chr4:20098747-20098758 chr4:20098736-20098747
20	CEBPB	chr4:19933278-19933565	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:19916399-19916665	A549	lung:	n/a	chr4:19916483-19916494 chr4:19916484-19916495
22	CEBPB	chr4:20047823-20048092	A549	lung:	n/a	n/a
23	CEBPB	chr4:19896103-19896389	HepG2	liver:	n/a	chr4:19896244-19896255
24	CEBPB	chr4:19808858-19809497	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:20047762-20048133	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:19916328-19916658	HepG2	liver:	n/a	chr4:19916483-19916494 chr4:19916484-19916495
27	CEBPB	chr4:19896101-19896417	IMR90	lung:	n/a	chr4:19896244-19896255
28	CEBPB	chr4:20047713-20048219	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:19936466-19936898	IMR90	lung:	n/a	chr4:19936776-19936787
30	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
31	CEBPB	chr4:19916368-19916576	K562	blood:	n/a	chr4:19916483-19916494 chr4:19916484-19916495
32	CEBPB	chr4:19980803-19981133	IMR90	lung:	n/a	chr4:19980961-19980972
33	CEBPB	chr4:19916304-19916655	IMR90	lung:	n/a	chr4:19916483-19916494 chr4:19916484-19916495
34	CEBPB	chr4:19946021-19946186	H1-hESC	embryonic stem cell:	n/a	chr4:19946085-19946098
35	CEBPB	chr4:20088528-20088955	HCT-116	colon:	n/a	n/a
36	CEBPB	chr4:20017605-20017805	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:20088402-20088983	HCT-116	colon:	n/a	n/a
38	CEBPB	chr4:19807640-19807945	IMR90	lung:	n/a	chr4:19807795-19807806 chr4:19807861-19807873 chr4:19807795-19807808
39	CEBPB	chr4:19843180-19843400	A549	lung:	n/a	chr4:19843221-19843232
40	CEBPB	chr4:20046288-20046755	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:20047769-20048129	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:20046045-20046765	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:20088542-20088852	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:19808756-19809489	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:20017474-20017897	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:19813832-19814087	IMR90	lung:	n/a	chr4:19813957-19813968 chr4:19813957-19813968 chr4:19813899-19813912
47	CEBPB	chr4:20030045-20030676	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr4:20091618-20091843	IMR90	lung:	n/a	chr4:20091693-20091706
49	CEBPB	chr4:19843110-19843405	HepG2	liver:	n/a	chr4:19843221-19843232
50	CEBPB	chr4:20017490-20017845	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:19984063-19984113	GM12891	blood:	n/a
2	chr4:20018421-20018471	SK-N-SH_RA	brain:	n/a
3	chr4:20006267-20006317	NHDF-neo	bronchial:	n/a
4	chr4:20006267-20006317	HepG2	liver:	n/a
5	chr4:20006267-20006317	NHBE	bronchial:	n/a
6	chr4:20006267-20006317	HAEpiC	amniotic membrane:	n/a
7	chr4:19962859-19962909	PFSK-1	brain:	n/a
8	chr4:20006267-20006317	RPTEC	kidney:	n/a
9	chr4:19984063-19984113	BE2_C	brain:	n/a
10	chr4:19962859-19962909	Caco-2	colon:	n/a
11	chr4:20006267-20006317	SK-N-SH_RA	brain:	n/a
12	chr4:20006267-20006317	AoSMC	blood vessel:	n/a
13	chr4:20018421-20018471	AG04450	lung:	fetal
14	chr4:20006267-20006317	BE2_C	brain:	n/a
15	chr4:20006267-20006317	HCM	heart:	n/a
16	chr4:20006267-20006317	HEK293	kidney:	embryo
17	chr4:19984063-19984113	SKMC	muscle:	n/a
18	chr4:20006267-20006317	HEEpiC	esophagus:	n/a
19	chr4:19962859-19962909	HepG2	liver:	n/a
20	chr4:20018421-20018471	MCF10A-Er-Src	breast:	n/a
21	chr4:20006267-20006317	NT2-D1	testis:	n/a
22	chr4:20018421-20018471	U87	brain:	n/a
23	chr4:20018421-20018471	K562	blood:	n/a
24	chr4:19984063-19984113	HEEpiC	esophagus:	n/a
25	chr4:19962859-19962909	MCF10A-Er-Src	breast:	n/a
26	chr4:19962859-19962909	NHDF-neo	bronchial:	n/a
27	chr4:20044588-20044638	HEK293	kidney:	embryo
28	chr4:19984063-19984113	Caco-2	colon:	n/a
29	chr4:19962859-19962909	PrEC	prostate:	n/a
30	chr4:19984063-19984113	HEK293	kidney:	embryo
31	chr4:20044588-20044638	NHDF-neo	bronchial:	n/a
32	chr4:19962859-19962909	HPAEpiC	pulmonary alveolar:	n/a
33	chr4:20018421-20018471	NHDF-neo	bronchial:	n/a
34	chr4:19962859-19962909	K562	blood:	n/a
35	chr4:19984063-19984113	SAEC	small airway:	n/a
36	chr4:19984063-19984113	HRE	kidney:	n/a
37	chr4:20018421-20018471	PANC-1	pancreas:	n/a
38	chr4:20044588-20044638	ECC-1	luminal epithelium:	n/a
39	chr4:19962859-19962909	HCPEpiC	choroid plexus:	n/a
40	chr4:19984063-19984113	ovcar-3	ovarian:	n/a
41	chr4:20006267-20006317	GM06990	blood:	n/a
42	chr4:19984063-19984113	NT2-D1	testis:	n/a
43	chr4:20018421-20018471	SK-N-MC	brain:	n/a
44	chr4:20044588-20044638	ovcar-3	ovarian:	n/a
45	chr4:19962859-19962909	HEK293	kidney:	embryo
46	chr4:19984063-19984113	AG04449	skin:	fetal
47	chr4:20006267-20006317	H1-hESC	embryonic stem cell:	embryo
48	chr4:20006267-20006317	SKMC	muscle:	n/a
49	chr4:19984063-19984113	AG04450	lung:	fetal
50	chr4:20006267-20006317	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20064153..20065819-chr4:20071734..20073623,2	K562	blood:
2	chr4:20063520..20065653-chr4:20071734..20074613,2	K562	blood:
3	chr4:20087439..20089887-chr4:20127144..20130135,2	K562	blood:
4	chr4:20063520..20065653-chr4:20071734..20074613,2	K562	blood:
5	chr4:20064153..20065819-chr4:20071734..20073623,2	K562	blood:
6	chr4:19788930..19791158-chr4:19794175..19796183,2	MCF-7	breast:
7	chr4:19835706..19836351-chr5:9383849..9384559,2	MCF-7	breast:
8	chr4:19788930..19791158-chr4:19794175..19796183,2	MCF-7	breast:
9	chr4:20025908..20028659-chr4:20253195..20254796,2	MCF-7	breast:

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

Variant related genes	Relation type
ENSG00000250611	TF binding region
ENSG00000241612	TF binding region
ENSG00000250611	CpG island
ENSG00000241612	CpG island

Extended variants
information (count: 5419 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5419 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149319290	chr4:19792803-19792804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576603727	chr4:19792806-19792807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111261431	chr4:19792810-19792811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs62296270	chr4:19792811-19792812	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs144623391	chr4:19792856-19792857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540987469	chr4:19792922-19792923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183619609	chr4:19792935-19792936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550662352	chr4:19792949-19792950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74724264	chr4:19792988-19792989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575038450	chr4:19792991-19792992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371057165	chr4:19792994-19792995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577668173	chr4:19793012-19793013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551881584	chr4:19793047-19793048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs62296271	chr4:19793063-19793064	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs190554285	chr4:19793089-19793090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116150222	chr4:19793108-19793109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535755348	chr4:19793142-19793143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs193264002	chr4:19793145-19793146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565691417	chr4:19793150-19793151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139482533	chr4:19793170-19793171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370966448	chr4:19793189-19793190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs144205570	chr4:19793210-19793211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146080246	chr4:19793261-19793262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185382694	chr4:19793293-19793294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140073580	chr4:19793313-19793314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548996635	chr4:19793322-19793323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541347862	chr4:19793345-19793346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190327356	chr4:19793358-19793359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533401439	chr4:19793379-19793380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142376815	chr4:19793381-19793382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181494494	chr4:19793410-19793411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530910467	chr4:19793411-19793412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs549959582	chr4:19793426-19793427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539834323	chr4:19793461-19793462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375825877	chr4:19793566-19793567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569042021	chr4:19793567-19793568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs112977509	chr4:19793599-19793600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs151295049	chr4:19793632-19793633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs10033221	chr4:19793639-19793640	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs537595594	chr4:19793640-19793641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372144635	chr4:19793641-19793642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185834435	chr4:19793746-19793747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10001502	chr4:19793917-19793918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188588379	chr4:19793946-19793947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181062415	chr4:19793953-19793954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs58143508	chr4:19793971-19793972	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs140569799	chr4:19794014-19794015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562061759	chr4:19794033-19794034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573924926	chr4:19794063-19794064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186042092	chr4:19794080-19794081	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
Colorectal cancer	16774939	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:19792800-19793200	Enhancers	Spleen	Spleen
2	chr4:19792800-19794400	Enhancers	HUVEC	blood vessel
3	chr4:19804800-19805600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:19804800-19805600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:19805200-19805600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:19805200-19805600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:19805400-19805600	Enhancers	Placenta Amnion	Placenta Amnion
8	chr4:19805600-19808200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr4:19805600-19809800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr4:19805800-19807600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr4:19807400-19807800	Enhancers	Primary hematopoietic stem cells	blood
12	chr4:19807400-19808800	Enhancers	Fetal Lung	lung
13	chr4:19807600-19808000	Enhancers	Placenta Amnion	Placenta Amnion
14	chr4:19807800-19808200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr4:19808000-19808400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr4:19808200-19809200	Enhancers	Fetal Kidney	kidney
17	chr4:19808200-19809400	Enhancers	Primary hematopoietic stem cells	blood
18	chr4:19808200-19810000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:19808200-19810200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:19808400-19808600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr4:19808400-19808800	Enhancers	Fetal Stomach	stomach
22	chr4:19808400-19809200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:19808400-19809400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:19808400-19809600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr4:19808400-19810000	Enhancers	Osteobl	bone
26	chr4:19808600-19808800	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr4:19808600-19808800	Enhancers	NHDF-Ad	bronchial
28	chr4:19808600-19809600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr4:19808600-19809600	Enhancers	NH-A	brain
30	chr4:19808600-19809800	Enhancers	NHLF	lung
31	chr4:19808800-19809400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr4:19808800-19809600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:19808800-19809600	Weak transcription	NHDF-Ad	bronchial
34	chr4:19808800-19811000	Weak transcription	Fetal Lung	lung
35	chr4:19809000-19809400	Enhancers	Fetal Stomach	stomach
36	chr4:19809000-19809800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:19809400-19813600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:19809600-19810800	Enhancers	Placenta Amnion	Placenta Amnion
39	chr4:19809600-19810800	Weak transcription	NH-A	brain
40	chr4:19809600-19811000	Enhancers	NHDF-Ad	bronchial
41	chr4:19809800-19810000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr4:19809800-19811800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:19810000-19810400	Weak transcription	Osteobl	bone
44	chr4:19810000-19810800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr4:19810000-19811800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:19810200-19810800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:19810400-19811400	Enhancers	Osteobl	bone
48	chr4:19810800-19811000	Enhancers	Fetal Stomach	stomach
49	chr4:19810800-19811400	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr4:19810800-19811400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links