Variant report

Variant	nsv899030
Chromosome Location	chr12:40509341-40580440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:546)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:40546628-40546911	K562	blood:	n/a	n/a
2	ATF2	chr12:40511589-40512134	GM12878	blood:	n/a	n/a
3	ATF2	chr12:40561772-40562281	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40511602-40512071	GM12878	blood:	n/a	n/a
5	ATF2	chr12:40562547-40563179	GM12878	blood:	n/a	n/a
6	ATF2	chr12:40562517-40563164	GM12878	blood:	n/a	n/a
7	ATF2	chr12:40530977-40531485	GM12878	blood:	n/a	n/a
8	ATF2	chr12:40561760-40562320	GM12878	blood:	n/a	n/a
9	BATF	chr12:40562718-40563113	GM12878	blood:	n/a	n/a
10	BATF	chr12:40531152-40531342	GM12878	blood:	n/a	n/a
11	BATF	chr12:40511643-40512006	GM12878	blood:	n/a	n/a
12	BATF	chr12:40562763-40563054	GM12878	blood:	n/a	n/a
13	BATF	chr12:40561850-40562111	GM12878	blood:	n/a	chr12:40562020-40562031
14	BATF	chr12:40511607-40511993	GM12878	blood:	n/a	n/a
15	BATF	chr12:40561861-40562191	GM12878	blood:	n/a	chr12:40562020-40562031
16	BCL11A	chr12:40511628-40512004	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:40562744-40562991	GM12878	blood:	n/a	chr12:40562817-40562826
18	BCL11A	chr12:40561855-40562181	GM12878	blood:	n/a	chr12:40562020-40562029 chr12:40562019-40562028
19	BCL11A	chr12:40562639-40563067	GM12878	blood:	n/a	chr12:40562817-40562826
20	BCLAF1	chr12:40562599-40563097	GM12878	blood:	n/a	chr12:40562817-40562826
21	BCLAF1	chr12:40511651-40511942	GM12878	blood:	n/a	n/a
22	BCLAF1	chr12:40511645-40512023	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:40531157-40531393	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:40561787-40563459	GM12878	blood:	n/a	n/a
25	CEBPB	chr12:40543763-40544037	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:40558987-40559278	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:40551397-40551659	A549	lung:	n/a	chr12:40551504-40551513 chr12:40551502-40551515
28	CEBPB	chr12:40552448-40552556	A549	lung:	n/a	n/a
29	CEBPB	chr12:40535738-40536586	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:40517397-40517597	HepG2	liver:	n/a	n/a
31	CEBPB	chr12:40533238-40533525	HepG2	liver:	n/a	chr12:40533360-40533371
32	CEBPB	chr12:40543731-40544102	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:40517338-40517663	Hela-S3	cervix:	n/a	chr12:40517645-40517657
34	CEBPB	chr12:40564027-40564186	A549	lung:	n/a	chr12:40564105-40564116
35	CEBPB	chr12:40517339-40517624	A549	lung:	n/a	n/a
36	CEBPB	chr12:40533224-40533424	A549	lung:	n/a	chr12:40533360-40533371
37	CEBPB	chr12:40565470-40565502	A549	lung:	n/a	n/a
38	CEBPB	chr12:40562546-40563162	GM12878	blood:	n/a	n/a
39	CEBPB	chr12:40558991-40559285	A549	lung:	n/a	n/a
40	CHD1	chr12:40552572-40552917	GM12878	blood:	n/a	n/a
41	CHD2	chr12:40562672-40563107	GM12878	blood:	n/a	n/a
42	CHD2	chr12:40549674-40549874	GM12878	blood:	n/a	n/a
43	CHD2	chr12:40570471-40570477	GM12878	blood:	n/a	n/a
44	CREB1	chr12:40531137-40531390	GM12878	blood:	n/a	n/a
45	CREB1	chr12:40562700-40563169	GM12878	blood:	n/a	n/a
46	CREB1	chr12:40561823-40562211	GM12878	blood:	n/a	n/a
47	CTCF	chr12:40546658-40546872	GM10248	blood:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
48	CTCF	chr12:40546674-40546849	NHEK	skin:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
49	CTCF	chr12:40546720-40546870	HCT-116	colon:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793
50	CTCF	chr12:40546660-40546810	GM12872	blood:	n/a	chr12:40546776-40546792 chr12:40546777-40546798 chr12:40546778-40546791 chr12:40546775-40546793

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40548738-40548788	SKMC	muscle:	n/a
2	chr12:40548738-40548788	AoSMC	blood vessel:	n/a
3	chr12:40548738-40548788	Hela-S3	cervix:	n/a
4	chr12:40548738-40548788	AG09309	skin:	n/a
5	chr12:40548738-40548788	BJ	skin:	n/a
6	chr12:40548738-40548788	AG04449	skin:	fetal
7	chr12:40548738-40548788	A549	lung:	n/a
8	chr12:40548738-40548788	NT2-D1	testis:	n/a
9	chr12:40548738-40548788	IMR90	lung:	fetal
10	chr12:40548738-40548788	H1-hESC	embryonic stem cell:	embryo
11	chr12:40548738-40548788	SK-N-SH_RA	brain:	n/a
12	chr12:40548738-40548788	MCF10A-Er-Src	breast:	n/a
13	chr12:40548738-40548788	PFSK-1	brain:	n/a
14	chr12:40548738-40548788	ovcar-3	ovarian:	n/a
15	chr12:40548738-40548788	HRPEpiC	eye:	n/a
16	chr12:40548738-40548788	GM12878	blood:	n/a
17	chr12:40548738-40548788	K562	blood:	n/a
18	chr12:40548738-40548788	NHBE	bronchial:	n/a
19	chr12:40548738-40548788	SAEC	small airway:	n/a
20	chr12:40548738-40548788	ProgFib	skin:	n/a
21	chr12:40548738-40548788	LNCaP	prostate:	n/a
22	chr12:40548738-40548788	GM06990	blood:	n/a
23	chr12:40548738-40548788	AG04450	lung:	fetal
24	chr12:40548738-40548788	GM12891	blood:	n/a
25	chr12:40548738-40548788	Hepatocyte	liver:	n/a
26	chr12:40548738-40548788	HCF	heart:	n/a
27	chr12:40548738-40548788	AG10803	skin:	n/a
28	chr12:40548738-40548788	HPAEpiC	pulmonary alveolar:	n/a
29	chr12:40548738-40548788	PANC-1	pancreas:	n/a
30	chr12:40548738-40548788	HCPEpiC	choroid plexus:	n/a
31	chr12:40548738-40548788	Jurkat	blood:	n/a
32	chr12:40548738-40548788	HCT-116	colon:	n/a
33	chr12:40548738-40548788	HRCEpiC	kidney:	n/a
34	chr12:40548738-40548788	NB4	blood:	n/a
35	chr12:40548738-40548788	HEK293	kidney:	embryo
36	chr12:40548738-40548788	Caco-2	colon:	n/a
37	chr12:40548738-40548788	HepG2	liver:	n/a
38	chr12:40548738-40548788	CMK	blood:	n/a
39	chr12:40548738-40548788	HNPCEpiC	eye:	n/a
40	chr12:40548738-40548788	RPTEC	kidney:	n/a
41	chr12:40548738-40548788	HAEpiC	amniotic membrane:	n/a
42	chr12:40548738-40548788	PrEC	prostate:	n/a
43	chr12:40548738-40548788	U87	brain:	n/a
44	chr12:40548738-40548788	GM12892	blood:	n/a
45	chr12:40548738-40548788	MCF-7	breast:	n/a
46	chr12:40548738-40548788	HIPEpiC	eye:	n/a
47	chr12:40548738-40548788	HMEC	breast:	n/a
48	chr12:40548738-40548788	HRE	kidney:	n/a
49	chr12:40548738-40548788	GM19239	blood:	n/a
50	chr12:40548738-40548788	AG09319	gingival:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	12:40545640-40549031..12:40703633-40711447	GM12878	blood:
2	chr12:40546325..40546967-chr12:40662693..40663558,3	MCF-7	breast:
3	chr12:40526853..40529105-chr12:40530805..40532717,2	MCF-7	breast:
4	chr12:40536767..40538493-chr12:40545018..40546756,2	K562	blood:
5	chr12:40546299..40547451-chr12:40706483..40707430,5	MCF-7	breast:
6	chr1:169315069..169315689-chr12:40537506..40538182,2	MCF-7	breast:
7	12:40543943-40545640..12:40703633-40711447	GM12878	blood:
8	12:40545640-40549031..12:40691796-40694737	GM12878	blood:
9	12:40551632-40552246..12:40691796-40694737	GM12878	blood:
10	chr12:40526853..40529105-chr12:40530805..40532717,2	MCF-7	breast:
11	chr10:125795379..125796137-chr12:40561478..40561982,2	MCF-7	breast:
12	chr12:40520984..40522789-chr12:40525869..40527665,2	K562	blood:
13	chr12:40546236..40547437-chr12:40706403..40707441,12	MCF-7	breast:
14	chr12:40536767..40538493-chr12:40545018..40546756,2	K562	blood:
15	chr12:40520984..40522789-chr12:40525869..40527665,2	K562	blood:
16	chr12:40158520..40159448-chr12:40546284..40547792,5	MCF-7	breast:
17	12:40560427-40561510..12:40703633-40711447	GM12878	blood:
18	12:40517820-40521124..12:40703633-40711447	GM12878	blood:
19	12:40570708-40576790..12:40691796-40694737	K562	blood:
20	12:40525880-40532672..12:40703633-40711447	GM12878	blood:
21	12:40551632-40552246..12:40703633-40711447	GM12878	blood:
22	chr12:40543659..40545848-chr12:40705219..40707677,2	MCF-7	breast:
23	12:40570708-40576790..12:40703633-40711447	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A13-1	chr12:40552238-40552325	XLOC_010052
2	lnc-LRRK2-1	chr12:40549559-40550164	NONHSAT027720
3	lnc-LRRK2-1	chr12:40550041-40550145	XLOC_009712
4	lnc-SLC2A13-1	chr12:40551656-40551857	XLOC_010052
5	lnc-LRRK2-1	chr12:40561049-40561678	NONHSAT027720
6	lnc-SLC2A13-1	chr12:40534259-40536436	XLOC_010052
7	lnc-SLC2A13-1	chr12:40545831-40545945	XLOC_010052
8	lnc-LRRK2-1	chr12:40561050-40561509	XLOC_009712
9	lnc-SLC2A13-2	chr12:40579811-40579985	XLOC_010053
10	lnc-LRRK2-1	chr12:40560054-40560152	XLOC_009712
11	lnc-SLC2A13-1	chr12:40537983-40538106	XLOC_010052
12	lnc-SLC2A13-1	chr12:40551656-40551857	XLOC_010052
13	lnc-SLC2A13-1	chr12:40534728-40536678	ENSG00000260943.1
14	lnc-LRRK2-1	chr12:40561050-40561414	XLOC_009712
15	lnc-SLC2A13-1	chr12:40552238-40552325	XLOC_010052
16	lnc-SLC2A13-1	chr12:40545831-40545945	XLOC_010052
17	lnc-LRRK2-1	chr12:40560053-40560152	NONHSAT027720
18	lnc-SLC2A13-1	chr12:40537621-40538106	XLOC_010052

No data

Variant related genes	Relation type
ENSG00000223914	TF binding region
ENSG00000260943	TF binding region
ENSG00000223914	CpG island
ENSG00000260943	CpG island
ENSG00000188906	chromatin interactions
BRSK1	miRNA target sites
SDCBP	miRNA target sites
NR3C1	miRNA target sites
BRMS1L	miRNA target sites
BRWD1	miRNA target sites

Extended variants
information (count: 2322 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2322 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12581285	chr12:40509341-40509342	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545844547	chr12:40509350-40509351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148673290	chr12:40509366-40509367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531750710	chr12:40509381-40509382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543780836	chr12:40509429-40509430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561970782	chr12:40509456-40509457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529586880	chr12:40509492-40509493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548127314	chr12:40509502-40509503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11175225	chr12:40509515-40509516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559948484	chr12:40509549-40509550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112263086	chr12:40509566-40509567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2638231	chr12:40509612-40509613	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs79469378	chr12:40509629-40509630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372620577	chr12:40509700-40509701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200181015	chr12:40509713-40509714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111845826	chr12:40509742-40509743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570517293	chr12:40509814-40509815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73093531	chr12:40509854-40509855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs151227451	chr12:40509950-40509951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567978074	chr12:40509963-40509964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139234373	chr12:40510022-40510023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553652875	chr12:40510026-40510027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572053601	chr12:40510030-40510031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190694681	chr12:40510084-40510085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181167908	chr12:40510087-40510088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532476583	chr12:40510088-40510089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543576346	chr12:40510097-40510098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562082372	chr12:40510160-40510161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115531882	chr12:40510165-40510166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373937698	chr12:40510179-40510180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541700661	chr12:40510183-40510184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368650470	chr12:40511043-40511044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs372638097	chr12:40511076-40511077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559176447	chr12:40511111-40511112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1482288	chr12:40511183-40511184	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs578242891	chr12:40511232-40511233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17458570	chr12:40511283-40511284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545392030	chr12:40511340-40511341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188635025	chr12:40511372-40511373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1117378	chr12:40511467-40511468	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs543250316	chr12:40511480-40511481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561436354	chr12:40511514-40511515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs17489750	chr12:40511522-40511523	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs546964276	chr12:40511633-40511634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192325352	chr12:40511644-40511645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2708452	chr12:40511647-40511648	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542175373	chr12:40511708-40511709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182864124	chr12:40511732-40511733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569787908	chr12:40511737-40511738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187505405	chr12:40511738-40511739	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40501200-40510200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:40509200-40509400	Enhancers	Aorta	Aorta
3	chr12:40511000-40512400	Enhancers	GM12878-XiMat	blood
4	chr12:40517000-40517600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr12:40517000-40518000	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr12:40517200-40517600	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr12:40520400-40522200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr12:40521200-40521600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr12:40526800-40527200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr12:40526800-40527400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:40530600-40531400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
12	chr12:40530600-40531400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:40530600-40531600	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr12:40530600-40531600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr12:40530800-40531200	Enhancers	Primary B cells from peripheral blood	blood
16	chr12:40530800-40531400	Enhancers	GM12878-XiMat	blood
17	chr12:40530800-40532000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr12:40531000-40531400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr12:40531000-40531400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:40531000-40531400	Enhancers	HUVEC	blood vessel
21	chr12:40531000-40531600	Enhancers	Primary B cells from cord blood	blood
22	chr12:40531200-40531600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr12:40531200-40531800	Enhancers	NHDF-Ad	bronchial
24	chr12:40531200-40532000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr12:40531200-40532400	Enhancers	HMEC	breast
26	chr12:40531400-40532600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:40531400-40532600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:40531400-40532600	Enhancers	NHEK	skin
29	chr12:40531600-40532800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:40531800-40532800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:40532400-40535600	Weak transcription	HMEC	breast
32	chr12:40532600-40535600	Weak transcription	NHEK	skin
33	chr12:40532600-40535800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:40532800-40535800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr12:40532800-40543800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:40533200-40533400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr12:40535000-40537200	Enhancers	Hela-S3	cervix
38	chr12:40535600-40536600	Enhancers	HMEC	breast
39	chr12:40535600-40536600	Enhancers	NHEK	skin
40	chr12:40535800-40536400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:40535800-40536400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:40536000-40536600	Enhancers	Placenta Amnion	Placenta Amnion
43	chr12:40540800-40541400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr12:40541000-40541800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr12:40541200-40541400	Enhancers	Aorta	Aorta
46	chr12:40541400-40546600	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr12:40541800-40546600	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr12:40543400-40544000	Enhancers	Adipose Nuclei	Adipose
49	chr12:40543400-40544200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr12:40543600-40543800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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