Variant report

Variant	nsv1052661
Chromosome Location	chr12:40603049-40642812
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	ATF2	chr12:40619916-40620447	GM12878	blood:	n/a	n/a
2	ATF2	chr12:40626439-40626762	GM12878	blood:	n/a	n/a
3	ATF2	chr12:40619878-40620536	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40626340-40626772	GM12878	blood:	n/a	n/a
5	BACH1	chr12:40612892-40612903	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr12:40618314-40618959	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr12:40620474-40620707	GM12878	blood:	n/a	chr12:40620577-40620588
8	BATF	chr12:40619951-40620402	GM12878	blood:	n/a	chr12:40620016-40620024
9	BATF	chr12:40619967-40620344	GM12878	blood:	n/a	chr12:40620016-40620024
10	BCL11A	chr12:40618597-40619027	GM12878	blood:	n/a	chr12:40618849-40618857 chr12:40618818-40618831
11	BCL11A	chr12:40619935-40620396	GM12878	blood:	n/a	chr12:40620012-40620021 chr12:40620179-40620188
12	BCL11A	chr12:40619996-40620353	GM12878	blood:	n/a	chr12:40620012-40620021 chr12:40620179-40620188
13	BCL3	chr12:40618628-40618973	GM12878	blood:	n/a	chr12:40618849-40618857 chr12:40618818-40618831
14	BCL3	chr12:40620020-40620397	GM12878	blood:	n/a	chr12:40620179-40620188
15	BCLAF1	chr12:40618574-40619091	GM12878	blood:	n/a	chr12:40618849-40618857 chr12:40618818-40618831
16	BCLAF1	chr12:40618525-40618992	GM12878	blood:	n/a	chr12:40618849-40618857 chr12:40618818-40618831
17	BCLAF1	chr12:40619904-40620434	GM12878	blood:	n/a	chr12:40620012-40620021 chr12:40620179-40620188
18	BCLAF1	chr12:40620014-40620432	GM12878	blood:	n/a	chr12:40620179-40620188
19	BHLHE40	chr12:40619850-40620471	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:40618428-40619399	GM12878	blood:	n/a	chr12:40618496-40618512 chr12:40618745-40618761 chr12:40618493-40618509 chr12:40618858-40618874
21	BRCA1	chr12:40618900-40618955	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr12:40642410-40642763	HCT-116	colon:	n/a	n/a
23	CCNT2	chr12:40618511-40618711	K562	blood:	n/a	n/a
24	CEBPB	chr12:40616106-40616408	IMR90	lung:	n/a	chr12:40616288-40616299
25	CEBPB	chr12:40619408-40619855	A549	lung:	n/a	chr12:40619599-40619608 chr12:40619597-40619610 chr12:40619598-40619609 chr12:40619599-40619608 chr12:40619599-40619608
26	CEBPB	chr12:40619462-40619788	H1-hESC	embryonic stem cell:	n/a	chr12:40619599-40619608 chr12:40619597-40619610 chr12:40619598-40619609 chr12:40619599-40619608 chr12:40619599-40619608
27	CEBPB	chr12:40621180-40621515	A549	lung:	n/a	chr12:40621347-40621358
28	CEBPB	chr12:40619438-40619732	HepG2	liver:	n/a	chr12:40619599-40619608 chr12:40619597-40619610 chr12:40619598-40619609 chr12:40619599-40619608 chr12:40619599-40619608
29	CEBPB	chr12:40627858-40628014	H1-hESC	embryonic stem cell:	n/a	chr12:40627988-40627999 chr12:40627987-40627998
30	CEBPB	chr12:40609780-40610958	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr12:40627874-40628082	HepG2	liver:	n/a	chr12:40627988-40627999 chr12:40627987-40627998
32	CEBPB	chr12:40633038-40633067	A549	lung:	n/a	n/a
33	CEBPB	chr12:40630141-40630428	K562	blood:	n/a	chr12:40630267-40630278
34	CEBPB	chr12:40621221-40621449	HepG2	liver:	n/a	chr12:40621347-40621358
35	CEBPB	chr12:40623556-40623808	A549	lung:	n/a	n/a
36	CEBPB	chr12:40619412-40619785	IMR90	lung:	n/a	chr12:40619599-40619608 chr12:40619597-40619610 chr12:40619598-40619609 chr12:40619599-40619608 chr12:40619599-40619608
37	CEBPB	chr12:40619453-40619682	K562	blood:	n/a	chr12:40619599-40619608 chr12:40619597-40619610 chr12:40619598-40619609 chr12:40619599-40619608 chr12:40619599-40619608
38	CEBPB	chr12:40609814-40610138	A549	lung:	n/a	n/a
39	CEBPB	chr12:40637428-40637679	HepG2	liver:	n/a	chr12:40637648-40637660 chr12:40637549-40637562 chr12:40637549-40637560 chr12:40637549-40637562
40	CEBPB	chr12:40621177-40621516	IMR90	lung:	n/a	chr12:40621347-40621358
41	CEBPB	chr12:40631962-40632642	Hela-S3	cervix:	n/a	chr12:40632271-40632284
42	CEBPB	chr12:40630137-40630417	HepG2	liver:	n/a	chr12:40630267-40630278
43	CEBPB	chr12:40609787-40610136	IMR90	lung:	n/a	n/a
44	CEBPB	chr12:40616107-40616422	A549	lung:	n/a	chr12:40616288-40616299
45	CEBPB	chr12:40632127-40632489	A549	lung:	n/a	chr12:40632271-40632284
46	CEBPB	chr12:40609719-40610249	A549	lung:	n/a	n/a
47	CEBPB	chr12:40619419-40619781	Hela-S3	cervix:	n/a	chr12:40619599-40619608 chr12:40619597-40619610 chr12:40619598-40619609 chr12:40619599-40619608 chr12:40619599-40619608
48	CEBPB	chr12:40619102-40619954	A549	lung:	n/a	chr12:40619599-40619608 chr12:40619597-40619610 chr12:40619598-40619609 chr12:40619599-40619608 chr12:40619599-40619608
49	CEBPB	chr12:40630189-40630363	H1-hESC	embryonic stem cell:	n/a	chr12:40630267-40630278
50	CEBPB	chr12:40609844-40610088	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40622688-40622738	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:40622688-40622738	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:40618960-40619010	K562	blood:	n/a
4	chr12:40618782-40618832	NT2-D1	testis:	n/a
5	chr12:40618782-40618832	ECC-1	luminal epithelium:	n/a
6	chr12:40622688-40622738	HNPCEpiC	eye:	n/a
7	chr12:40618356-40618406	Jurkat	blood:	n/a
8	chr12:40618960-40619010	AG09309	skin:	n/a
9	chr12:40622688-40622738	NHBE	bronchial:	n/a
10	chr12:40618560-40618610	AG09319	gingival:	n/a
11	chr12:40618284-40618334	Hela-S3	cervix:	n/a
12	chr12:40618356-40618406	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:40619282-40619332	ECC-1	luminal epithelium:	n/a
14	chr12:40619282-40619332	HUVEC	blood vessel:	n/a
15	chr12:40618960-40619010	NHBE	bronchial:	n/a
16	chr12:40618782-40618832	AoSMC	blood vessel:	n/a
17	chr12:40622688-40622738	SKMC	muscle:	n/a
18	chr12:40618284-40618334	AG09319	gingival:	n/a
19	chr12:40619282-40619332	HRCEpiC	kidney:	n/a
20	chr12:40618356-40618406	NHBE	bronchial:	n/a
21	chr12:40618960-40619010	CMK	blood:	n/a
22	chr12:40618575-40618625	GM12891	blood:	n/a
23	chr12:40619282-40619332	Hela-S3	cervix:	n/a
24	chr12:40618782-40618832	LNCaP	prostate:	n/a
25	chr12:40618960-40619010	HPAEpiC	pulmonary alveolar:	n/a
26	chr12:40618284-40618334	GM12891	blood:	n/a
27	chr12:40618575-40618625	A549	lung:	n/a
28	chr12:40618782-40618832	SK-N-SH_RA	brain:	n/a
29	chr12:40618356-40618406	SAEC	small airway:	n/a
30	chr12:40618560-40618610	GM12892	blood:	n/a
31	chr12:40618575-40618625	HCM	heart:	n/a
32	chr12:40618960-40619010	HEEpiC	esophagus:	n/a
33	chr12:40618356-40618406	T-47D	breast:	n/a
34	chr12:40618560-40618610	HUVEC	blood vessel:	n/a
35	chr12:40622688-40622738	HEEpiC	esophagus:	n/a
36	chr12:40619282-40619332	PANC-1	pancreas:	n/a
37	chr12:40618960-40619010	HCF	heart:	n/a
38	chr12:40619282-40619332	HRPEpiC	eye:	n/a
39	chr12:40618284-40618334	GM19239	blood:	n/a
40	chr12:40618782-40618832	GM12878	blood:	n/a
41	chr12:40618782-40618832	K562	blood:	n/a
42	chr12:40618356-40618406	H1-hESC	embryonic stem cell:	embryo
43	chr12:40618575-40618625	NT2-D1	testis:	n/a
44	chr12:40618356-40618406	BE2_C	brain:	n/a
45	chr12:40618356-40618406	MCF-7	breast:	n/a
46	chr12:40618356-40618406	NB4	blood:	n/a
47	chr12:40618560-40618610	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:40618560-40618610	ECC-1	luminal epithelium:	n/a
49	chr12:40618782-40618832	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:40618560-40618610	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:40615913..40618239-chr12:40619276..40621204,2	K562	blood:
2	chr12:40597517..40600322-chr12:40605533..40608551,3	K562	blood:
3	12:40610100-40613194..12:40793507-40812339	K562	blood:
4	chr12:40615913..40618239-chr12:40619276..40621204,2	K562	blood:
5	chr12:40611277..40614132-chr12:40614284..40617171,2	K562	blood:
6	chr12:40619170..40621140-chr12:40621940..40624766,2	MCF-7	breast:
7	chr12:40616874..40619503-chr12:40632557..40634590,2	MCF-7	breast:
8	chr12:40611277..40614132-chr12:40614284..40617171,2	K562	blood:
9	chr11:64879233..64879808-chr12:40616252..40617103,2	NB4	blood:
10	chr11:62622983..62623761-chr12:40618210..40619016,2	NB4	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A13-2	chr12:40617461-40617605	XLOC_010053

Variant related genes	Relation type
LRRK2	TF binding region
ENSG00000225342	TF binding region
LRRK2	CpG island
ENSG00000225342	CpG island
ENSG00000188906	chromatin interactions
ENSG00000205592	chromatin interactions
ENSG00000255717	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000149809	chromatin interactions
ENSG00000225342	chromatin interactions

Extended variants
information (count: 1578 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1578 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533880150	chr12:40603065-40603066	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs558541616	chr12:40603088-40603089	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs570483599	chr12:40603115-40603116	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs538102356	chr12:40603166-40603167	Flanking Active TSS Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs17465653	chr12:40603224-40603225	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556168132	chr12:40603301-40603302	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2279535	chr12:40603316-40603317	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs12305120	chr12:40603321-40603322	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs76524269	chr12:40603349-40603350	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572161166	chr12:40603389-40603390	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545917997	chr12:40603405-40603406	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566325991	chr12:40603408-40603409	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564108637	chr12:40603461-40603462	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183838498	chr12:40603477-40603478	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs543828786	chr12:40603491-40603492	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12305241	chr12:40603509-40603510	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554802118	chr12:40603516-40603517	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs148428758	chr12:40603573-40603574	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188565121	chr12:40603590-40603591	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs373481984	chr12:40603624-40603625	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs559989413	chr12:40603629-40603630	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs118075840	chr12:40603676-40603677	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs560862725	chr12:40603710-40603711	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs537072924	chr12:40603717-40603718	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs181359220	chr12:40603718-40603719	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs12306744	chr12:40603719-40603720	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549789662	chr12:40603822-40603823	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185927156	chr12:40603825-40603826	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568224268	chr12:40603858-40603859	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535744259	chr12:40603868-40603869	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553525772	chr12:40603920-40603921	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142406585	chr12:40603925-40603926	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs2708429	chr12:40603957-40603958	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557810658	chr12:40603985-40603986	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576174373	chr12:40604002-40604003	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543441794	chr12:40604022-40604023	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562121166	chr12:40604029-40604030	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191175398	chr12:40604030-40604031	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181996106	chr12:40604041-40604042	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113303616	chr12:40604057-40604058	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541731187	chr12:40604067-40604068	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2638229	chr12:40604068-40604069	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs2638230	chr12:40604075-40604076	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552029914	chr12:40604120-40604121	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529614709	chr12:40604125-40604126	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146862046	chr12:40604133-40604134	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576630690	chr12:40604182-40604183	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571949477	chr12:40604207-40604208	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs61931633	chr12:40604282-40604283	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs568070037	chr12:40604321-40604322	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40601400-40604400	Enhancers	Primary B cells from peripheral blood	blood
2	chr12:40601600-40604400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr12:40602000-40603800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:40602200-40603800	Enhancers	GM12878-XiMat	blood
5	chr12:40602200-40604200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr12:40602200-40604200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr12:40602200-40604200	Enhancers	Fetal Kidney	kidney
8	chr12:40602200-40604400	Enhancers	Primary hematopoietic stem cells	blood
9	chr12:40602400-40604000	Enhancers	A549	lung
10	chr12:40602600-40603600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:40602800-40603200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
12	chr12:40602800-40603200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:40602800-40603200	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr12:40602800-40603400	Flanking Active TSS	Primary B cells from cord blood	blood
15	chr12:40602800-40603600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr12:40603000-40603800	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr12:40603000-40604400	Enhancers	Hela-S3	cervix
18	chr12:40603200-40604000	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr12:40603200-40604200	Enhancers	Colon Smooth Muscle	Colon
20	chr12:40603200-40605400	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr12:40603400-40604600	Enhancers	Primary B cells from cord blood	blood
22	chr12:40603600-40603800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr12:40603600-40604000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr12:40603600-40604200	Enhancers	Brain Hippocampus Middle	brain
25	chr12:40603800-40604200	Enhancers	HUVEC	blood vessel
26	chr12:40603800-40605400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr12:40604000-40604200	Flanking Active TSS	A549	lung
28	chr12:40604200-40604400	Active TSS	A549	lung
29	chr12:40604200-40609200	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr12:40604200-40611000	Weak transcription	Fetal Kidney	kidney
31	chr12:40604400-40605000	Weak transcription	A549	lung
32	chr12:40604400-40605800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr12:40604400-40609400	Weak transcription	Hela-S3	cervix
34	chr12:40605000-40605200	Enhancers	A549	lung
35	chr12:40605200-40610400	Weak transcription	A549	lung
36	chr12:40605800-40609000	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr12:40608800-40611400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr12:40609000-40609200	Active TSS	Monocytes-CD14+_RO01746	blood
39	chr12:40609200-40610000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr12:40609200-40611200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr12:40609400-40610000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr12:40609400-40610800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:40609400-40611000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:40609400-40611000	Enhancers	Hela-S3	cervix
45	chr12:40609400-40611000	Enhancers	HMEC	breast
46	chr12:40609600-40609800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr12:40609600-40610000	Enhancers	Primary B cells from cord blood	blood
48	chr12:40609600-40610000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr12:40609600-40610400	Enhancers	NHEK	skin
50	chr12:40609600-40610600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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