Variant report

Variant	nsv1044685
Chromosome Location	chr12:40574460-40771612
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1984)
CpG islands
(count:610)
Chromatin interactive
region (count:36)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1984 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:40681210-40681513	HepG2	liver:	n/a	n/a
2	ATF2	chr12:40656402-40656862	GM12878	blood:	n/a	n/a
3	ATF2	chr12:40619916-40620447	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40655686-40656207	GM12878	blood:	n/a	n/a
5	ATF2	chr12:40626340-40626772	GM12878	blood:	n/a	n/a
6	ATF2	chr12:40626439-40626762	GM12878	blood:	n/a	n/a
7	ATF2	chr12:40586416-40587052	GM12878	blood:	n/a	n/a
8	ATF2	chr12:40595878-40596303	GM12878	blood:	n/a	n/a
9	ATF2	chr12:40586412-40587192	GM12878	blood:	n/a	n/a
10	ATF2	chr12:40707639-40708167	GM12878	blood:	n/a	n/a
11	ATF2	chr12:40655786-40656165	GM12878	blood:	n/a	n/a
12	ATF2	chr12:40619878-40620536	GM12878	blood:	n/a	n/a
13	ATF2	chr12:40656311-40656835	GM12878	blood:	n/a	n/a
14	ATF2	chr12:40707693-40708075	GM12878	blood:	n/a	n/a
15	ATF3	chr12:40680924-40681633	A549	lung:	n/a	n/a
16	ATF3	chr12:40680957-40681637	A549	lung:	n/a	n/a
17	BACH1	chr12:40618314-40618959	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:40612892-40612903	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr12:40586494-40587027	GM12878	blood:	n/a	n/a
20	BATF	chr12:40655828-40656026	GM12878	blood:	n/a	chr12:40655963-40655974
21	BATF	chr12:40619967-40620344	GM12878	blood:	n/a	chr12:40620016-40620024
22	BATF	chr12:40655840-40656023	GM12878	blood:	n/a	chr12:40655963-40655974
23	BATF	chr12:40656446-40656805	GM12878	blood:	n/a	n/a
24	BATF	chr12:40620474-40620707	GM12878	blood:	n/a	chr12:40620577-40620588
25	BATF	chr12:40707731-40708124	GM12878	blood:	n/a	chr12:40707752-40707761 chr12:40707963-40707974
26	BATF	chr12:40707717-40708130	GM12878	blood:	n/a	chr12:40707752-40707761 chr12:40707963-40707974
27	BATF	chr12:40656440-40656787	GM12878	blood:	n/a	n/a
28	BATF	chr12:40619951-40620402	GM12878	blood:	n/a	chr12:40620016-40620024
29	BCL11A	chr12:40595884-40596183	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:40618597-40619027	GM12878	blood:	n/a	chr12:40618849-40618857 chr12:40618818-40618831
31	BCL11A	chr12:40656391-40656827	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:40707762-40708143	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:40656497-40656736	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:40707747-40708026	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:40586465-40587065	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:40586564-40587015	GM12878	blood:	n/a	n/a
37	BCL11A	chr12:40619996-40620353	GM12878	blood:	n/a	chr12:40620012-40620021 chr12:40620179-40620188
38	BCL11A	chr12:40619935-40620396	GM12878	blood:	n/a	chr12:40620012-40620021 chr12:40620179-40620188
39	BCL11A	chr12:40595947-40596107	GM12878	blood:	n/a	n/a
40	BCL3	chr12:40586697-40586979	GM12878	blood:	n/a	n/a
41	BCL3	chr12:40680909-40681796	A549	lung:	n/a	n/a
42	BCL3	chr12:40620020-40620397	GM12878	blood:	n/a	chr12:40620179-40620188
43	BCL3	chr12:40680963-40681733	A549	lung:	n/a	n/a
44	BCL3	chr12:40618628-40618973	GM12878	blood:	n/a	chr12:40618849-40618857 chr12:40618818-40618831
45	BCLAF1	chr12:40620014-40620432	GM12878	blood:	n/a	chr12:40620179-40620188
46	BCLAF1	chr12:40586463-40586857	GM12878	blood:	n/a	n/a
47	BCLAF1	chr12:40618525-40618992	GM12878	blood:	n/a	chr12:40618849-40618857 chr12:40618818-40618831
48	BCLAF1	chr12:40619904-40620434	GM12878	blood:	n/a	chr12:40620012-40620021 chr12:40620179-40620188
49	BCLAF1	chr12:40656342-40656718	GM12878	blood:	n/a	n/a
50	BCLAF1	chr12:40618574-40619091	GM12878	blood:	n/a	chr12:40618849-40618857 chr12:40618818-40618831

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40618575-40618625	AG04449	skin:	fetal
2	chr12:40645170-40645220	GM06990	blood:	n/a
3	chr12:40618782-40618832	HEK293	kidney:	embryo
4	chr12:40747204-40747254	HEK293	kidney:	embryo
5	chr12:40619282-40619332	HUVEC	blood vessel:	n/a
6	chr12:40618782-40618832	SK-N-SH_RA	brain:	n/a
7	chr12:40618960-40619010	HCF	heart:	n/a
8	chr12:40618560-40618610	IMR90	lung:	fetal
9	chr12:40618356-40618406	Jurkat	blood:	n/a
10	chr12:40622688-40622738	PANC-1	pancreas:	n/a
11	chr12:40618960-40619010	PANC-1	pancreas:	n/a
12	chr12:40618560-40618610	NHBE	bronchial:	n/a
13	chr12:40618356-40618406	Hela-S3	cervix:	n/a
14	chr12:40622688-40622738	AG09319	gingival:	n/a
15	chr12:40618560-40618610	GM12892	blood:	n/a
16	chr12:40618960-40619010	HEEpiC	esophagus:	n/a
17	chr12:40618960-40619010	PFSK-1	brain:	n/a
18	chr12:40618575-40618625	HMEC	breast:	n/a
19	chr12:40618560-40618610	HRCEpiC	kidney:	n/a
20	chr12:40747204-40747254	ovcar-3	ovarian:	n/a
21	chr12:40618356-40618406	U87	brain:	n/a
22	chr12:40618356-40618406	HRE	kidney:	n/a
23	chr12:40618575-40618625	HRPEpiC	eye:	n/a
24	chr12:40618356-40618406	SK-N-MC	brain:	n/a
25	chr12:40747204-40747254	ECC-1	luminal epithelium:	n/a
26	chr12:40622688-40622738	NT2-D1	testis:	n/a
27	chr12:40618575-40618625	PrEC	prostate:	n/a
28	chr12:40618960-40619010	NH-A	brain:	n/a
29	chr12:40618284-40618334	AoSMC	blood vessel:	n/a
30	chr12:40618575-40618625	SK-N-SH_RA	brain:	n/a
31	chr12:40747204-40747254	HRCEpiC	kidney:	n/a
32	chr12:40618960-40619010	SK-N-MC	brain:	n/a
33	chr12:40618575-40618625	NB4	blood:	n/a
34	chr12:40619282-40619332	HAEpiC	amniotic membrane:	n/a
35	chr12:40618782-40618832	NB4	blood:	n/a
36	chr12:40618960-40619010	HCT-116	colon:	n/a
37	chr12:40618782-40618832	HEEpiC	esophagus:	n/a
38	chr12:40618560-40618610	HEK293	kidney:	embryo
39	chr12:40618575-40618625	ProgFib	skin:	n/a
40	chr12:40618284-40618334	IMR90	lung:	fetal
41	chr12:40619282-40619332	NT2-D1	testis:	n/a
42	chr12:40618560-40618610	PrEC	prostate:	n/a
43	chr12:40618356-40618406	SK-N-SH_RA	brain:	n/a
44	chr12:40618960-40619010	HUVEC	blood vessel:	n/a
45	chr12:40747204-40747254	NH-A	brain:	n/a
46	chr12:40618782-40618832	Hepatocyte	liver:	n/a
47	chr12:40618356-40618406	AG04450	lung:	fetal
48	chr12:40618356-40618406	ECC-1	luminal epithelium:	n/a
49	chr12:40618960-40619010	GM06990	blood:	n/a
50	chr12:40618575-40618625	AG09309	skin:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:40719199..40719744-chr12:41315365..41315912,2	MCF-7	breast:
2	12:40642938-40650987..12:40793507-40812339	K562	blood:
3	chr12:40658480..40661049-chr12:40663809..40666158,2	MCF-7	breast:
4	chr12:40615913..40618239-chr12:40619276..40621204,2	K562	blood:
5	chr12:40611277..40614132-chr12:40614284..40617171,2	K562	blood:
6	chr11:64879233..64879808-chr12:40616252..40617103,2	NB4	blood:
7	chr12:40597517..40600322-chr12:40605533..40608551,3	K562	blood:
8	12:40610100-40613194..12:40793507-40812339	K562	blood:
9	chr1:153939261..153941119-chr12:40643887..40646371,2	MCF-7	breast:
10	12:40583667-40584606..12:40703633-40711447	GM12878	blood:
11	chr12:40730810..40731494-chr12:40768592..40769125,2	MCF-7	breast:
12	chr12:40616874..40619503-chr12:40632557..40634590,2	MCF-7	breast:
13	12:40570708-40576790..12:40691796-40694737	K562	blood:
14	chr11:62622983..62623761-chr12:40618210..40619016,2	NB4	blood:
15	chr12:40718708..40719694-chr12:40730425..40731019,2	MCF-7	breast:
16	chr12:40718929..40719819-chr12:40768166..40769419,3	MCF-7	breast:
17	chr12:40718929..40719819-chr12:40768166..40769419,3	MCF-7	breast:
18	chr12:40597517..40600322-chr12:40605533..40608551,3	K562	blood:
19	chr12:40611277..40614132-chr12:40614284..40617171,2	K562	blood:
20	chr12:40619170..40621140-chr12:40621940..40624766,2	MCF-7	breast:
21	chr12:40730058..40730795-chr12:40768301..40769589,4	MCF-7	breast:
22	chr12:40715339..40716976-chr12:40720060..40722353,2	MCF-7	breast:
23	chr12:40730058..40730795-chr12:40768301..40769589,4	MCF-7	breast:
24	chr12:40615913..40618239-chr12:40619276..40621204,2	K562	blood:
25	12:40703633-40711447..12:40765226-40767074	GM12878	blood:
26	chr12:40718883..40719693-chr12:40958776..40959283,2	MCF-7	breast:
27	chr12:40718708..40719694-chr12:40730425..40731019,2	MCF-7	breast:
28	chr12:40546325..40546967-chr12:40662693..40663558,3	MCF-7	breast:
29	chr12:40768243..40769926-chr12:40782774..40784277,2	K562	blood:
30	chr12:40730810..40731494-chr12:40768592..40769125,2	MCF-7	breast:
31	chr12:40658480..40661049-chr12:40663809..40666158,2	MCF-7	breast:
32	chr12:40719158..40719845-chr12:40839913..40840458,2	MCF-7	breast:
33	12:40570708-40576790..12:40703633-40711447	K562	blood:
34	chr12:40721972..40722829-chr4:110621913..110622453,2	MCF-7	breast:
35	chr12:40715339..40716976-chr12:40720060..40722353,2	MCF-7	breast:
36	12:40716064-40722905..12:40793507-40812339	GM12878	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A13-2	chr12:40579811-40579985	XLOC_010053
2	lnc-SLC2A13-2	chr12:40617461-40617605	XLOC_010053
3	lnc-SLC2A13-2	chr12:40584055-40584196	XLOC_010053
4	lnc-SLC2A13-2	chr12:40582885-40583007	XLOC_010053

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LRRK2	hsa-miR-205-5p	chr12:40761670-40761690
2	LRRK2	hsa-miR-205-5p	chr12:40761683-40761690

Variant related genes	Relation type
ENSG00000229899	TF binding region
LRRK2	TF binding region
ENSG00000225342	TF binding region
ENSG00000229899	CpG island
LRRK2	CpG island
ENSG00000225342	CpG island
ENSG00000225342	chromatin interactions
ENSG00000255717	chromatin interactions
ENSG00000168003	chromatin interactions
ENSG00000188906	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000149809	chromatin interactions
ENSG00000143578	chromatin interactions
ENSG00000205592	chromatin interactions

Extended variants
information (count: 7977 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7977 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114405467	chr12:40574474-40574475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs371073957	chr12:40574479-40574480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs182241229	chr12:40574480-40574481	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545979727	chr12:40574532-40574533	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35887536	chr12:40574549-40574550	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537452190	chr12:40574588-40574589	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532056590	chr12:40574590-40574591	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550298779	chr12:40574715-40574716	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556400366	chr12:40574716-40574717	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs113943383	chr12:40574814-40574815	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs187539958	chr12:40574862-40574863	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs545558643	chr12:40574864-40574865	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146097617	chr12:40574964-40574965	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2244780	chr12:40574969-40574970	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs534141116	chr12:40575005-40575006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs142152735	chr12:40575006-40575007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs192467976	chr12:40575014-40575015	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184839477	chr12:40575029-40575030	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112147557	chr12:40575030-40575031	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs28365202	chr12:40575060-40575061	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574728682	chr12:40575062-40575063	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139872131	chr12:40575067-40575068	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs67671161	chr12:40575068-40575069	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs3057558	chr12:40575076-40575077	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201538008	chr12:40575077-40575078	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2708402	chr12:40575086-40575087	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs12581617	chr12:40575092-40575093	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs572647593	chr12:40575108-40575109	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11300948	chr12:40575137-40575138	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576033856	chr12:40575157-40575158	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546117007	chr12:40575158-40575159	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139408196	chr12:40575173-40575174	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2708403	chr12:40575217-40575218	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs184635705	chr12:40575224-40575225	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs562448931	chr12:40575231-40575232	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554927157	chr12:40575312-40575313	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529653534	chr12:40575332-40575333	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs562772716	chr12:40575342-40575343	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189905054	chr12:40575355-40575356	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560120290	chr12:40575409-40575410	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs200512742	chr12:40575431-40575432	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527565296	chr12:40575457-40575458	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150072557	chr12:40575506-40575507	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570631806	chr12:40575510-40575511	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs538041107	chr12:40575538-40575539	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550207297	chr12:40575546-40575547	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551536245	chr12:40575579-40575580	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs568453385	chr12:40575612-40575613	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566590200	chr12:40575621-40575622	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2708404	chr12:40575630-40575631	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:59)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1546 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40575200-40575800	Enhancers	Primary T cells fromperipheralblood	blood
2	chr12:40575200-40575800	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr12:40575200-40575800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr12:40575200-40575800	Enhancers	Primary T killer memory cells from peripheral blood	blood
5	chr12:40575200-40576000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr12:40575200-40576000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr12:40575200-40576000	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr12:40575200-40576000	Enhancers	HUVEC	blood vessel
9	chr12:40575200-40576200	Enhancers	Primary T cells from cord blood	blood
10	chr12:40575200-40576200	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr12:40575400-40575800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr12:40575600-40576000	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr12:40575600-40576200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr12:40577200-40577600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:40582200-40582600	Enhancers	Liver	Liver
16	chr12:40582200-40584800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:40583800-40584400	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
18	chr12:40584400-40586000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr12:40585600-40587200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr12:40585800-40586000	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr12:40585800-40587000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr12:40585800-40587200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:40585800-40587400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr12:40586000-40586200	Enhancers	GM12878-XiMat	blood
25	chr12:40586000-40586400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr12:40586000-40586800	Enhancers	Primary B cells from cord blood	blood
27	chr12:40586000-40586800	Enhancers	Primary B cells from peripheral blood	blood
28	chr12:40586000-40587000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr12:40586000-40587000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr12:40586000-40587400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr12:40586000-40587600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr12:40586000-40591000	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr12:40586200-40586600	Enhancers	Primary T cells from cord blood	blood
34	chr12:40586200-40586800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr12:40586200-40586800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:40586200-40587000	Active TSS	GM12878-XiMat	blood
37	chr12:40586200-40587200	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr12:40586200-40591600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr12:40586400-40587000	Enhancers	Primary hematopoietic stem cells	blood
40	chr12:40586400-40587000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr12:40586400-40587200	Enhancers	HUVEC	blood vessel
42	chr12:40586600-40587000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr12:40586600-40587200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:40586800-40587200	Flanking Active TSS	Primary B cells from cord blood	blood
45	chr12:40586800-40587200	Flanking Active TSS	Primary B cells from peripheral blood	blood
46	chr12:40586800-40588800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr12:40587000-40587400	Flanking Active TSS	GM12878-XiMat	blood
48	chr12:40587000-40587800	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr12:40587000-40588000	Weak transcription	Primary hematopoietic stem cells	blood
50	chr12:40587000-40588200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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