Variant report

Variant	nsv832378
Chromosome Location	chr12:40943111-41132305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1054)
CpG islands
(count:1403)
Chromatin interactive
region (count:14)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:41091506-41091600	K562	blood:	n/a	n/a
2	ATF2	chr12:40955261-40955752	GM12878	blood:	n/a	n/a
3	ATF2	chr12:41008630-41009189	GM12878	blood:	n/a	n/a
4	ATF2	chr12:41095495-41095972	GM12878	blood:	n/a	n/a
5	ATF2	chr12:40953520-40954269	GM12878	blood:	n/a	n/a
6	ATF2	chr12:41095553-41095922	GM12878	blood:	n/a	n/a
7	ATF2	chr12:40954996-40955723	GM12878	blood:	n/a	n/a
8	ATF2	chr12:41074934-41075291	GM12878	blood:	n/a	n/a
9	ATF2	chr12:41008640-41009227	GM12878	blood:	n/a	n/a
10	ATF2	chr12:40953538-40954231	GM12878	blood:	n/a	n/a
11	ATF3	chr12:41112137-41112996	A549	lung:	n/a	n/a
12	ATF3	chr12:41112133-41113026	A549	lung:	n/a	n/a
13	BACH1	chr12:41112882-41112949	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr12:41008148-41008581	GM12878	blood:	n/a	n/a
15	BATF	chr12:41095607-41095850	GM12878	blood:	n/a	n/a
16	BATF	chr12:41008782-41009071	GM12878	blood:	n/a	n/a
17	BATF	chr12:41095547-41095917	GM12878	blood:	n/a	n/a
18	BATF	chr12:41008719-41009067	GM12878	blood:	n/a	n/a
19	BATF	chr12:41009324-41009510	GM12878	blood:	n/a	chr12:41009441-41009452 chr12:41009425-41009436
20	BCL11A	chr12:41008808-41009013	GM12878	blood:	n/a	n/a
21	BCL11A	chr12:41008728-41009061	GM12878	blood:	n/a	n/a
22	BCL11A	chr12:41095533-41095952	GM12878	blood:	n/a	n/a
23	BCL3	chr12:41112128-41113731	A549	lung:	n/a	n/a
24	BCL3	chr12:41008714-41009163	GM12878	blood:	n/a	n/a
25	BCL3	chr12:41112152-41113088	A549	lung:	n/a	n/a
26	BCL3	chr12:40953531-40954178	GM12878	blood:	n/a	n/a
27	BCL3	chr12:40953675-40954068	GM12878	blood:	n/a	n/a
28	BCLAF1	chr12:41008687-41009212	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:40955455-40955598	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:41112220-41112589	A549	lung:	n/a	n/a
31	BHLHE40	chr12:41075076-41075141	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:41061948-41062165	A549	lung:	n/a	n/a
33	BRCA1	chr12:41016147-41016191	GM12878	blood:	n/a	n/a
34	CEBPB	chr12:41084252-41084501	MCF-7	breast:	n/a	n/a
35	CEBPB	chr12:40969826-40970115	HepG2	liver:	n/a	chr12:40970015-40970026 chr12:40969981-40969992
36	CEBPB	chr12:41008193-41008521	A549	lung:	n/a	chr12:41008352-41008363
37	CEBPB	chr12:41112226-41113067	A549	lung:	n/a	chr12:41112729-41112741
38	CEBPB	chr12:41113250-41113604	A549	lung:	n/a	n/a
39	CEBPB	chr12:41098590-41098896	A549	lung:	n/a	n/a
40	CEBPB	chr12:40969858-40970163	A549	lung:	n/a	chr12:40970015-40970026 chr12:40969981-40969992
41	CEBPB	chr12:41084203-41084776	A549	lung:	n/a	n/a
42	CEBPB	chr12:40969835-40970109	IMR90	lung:	n/a	chr12:40970015-40970026 chr12:40969981-40969992
43	CEBPB	chr12:40977556-40977925	HepG2	liver:	n/a	chr12:40977774-40977785
44	CEBPB	chr12:41084159-41084588	HCT-116	colon:	n/a	n/a
45	CEBPB	chr12:41005844-41006155	A549	lung:	n/a	n/a
46	CEBPB	chr12:41084168-41084583	A549	lung:	n/a	n/a
47	CEBPB	chr12:41111882-41113025	A549	lung:	n/a	chr12:41112729-41112741
48	CEBPB	chr12:41061715-41062241	A549	lung:	n/a	n/a
49	CEBPB	chr12:41026687-41027367	A549	lung:	n/a	chr12:41026909-41026920 chr12:41026908-41026921
50	CEBPB	chr12:41084053-41084569	A549	lung:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:41087092-41087142	AG09309	skin:	n/a
2	chr12:41085286-41085336	LNCaP	prostate:	n/a
3	chr12:41087101-41087151	AG04450	lung:	fetal
4	chr12:41087459-41087509	HCF	heart:	n/a
5	chr12:41086274-41086324	GM12892	blood:	n/a
6	chr12:41087092-41087142	NHDF-neo	bronchial:	n/a
7	chr12:41086800-41086850	SK-N-MC	brain:	n/a
8	chr12:41086282-41086332	HL-60	blood:	n/a
9	chr12:41087101-41087151	RPTEC	kidney:	n/a
10	chr12:41086365-41086415	CMK	blood:	n/a
11	chr12:41043074-41043124	AG04450	lung:	fetal
12	chr12:41086879-41086929	AoSMC	blood vessel:	n/a
13	chr12:41085302-41085352	K562	blood:	n/a
14	chr12:41083590-41083640	HCT-116	colon:	n/a
15	chr12:41087252-41087302	LNCaP	prostate:	n/a
16	chr12:41086227-41086277	ECC-1	luminal epithelium:	n/a
17	chr12:41086680-41086730	PANC-1	pancreas:	n/a
18	chr12:41086277-41086327	HRCEpiC	kidney:	n/a
19	chr12:41086800-41086850	NHBE	bronchial:	n/a
20	chr12:41087101-41087151	HCPEpiC	choroid plexus:	n/a
21	chr12:41087092-41087142	SK-N-SH_RA	brain:	n/a
22	chr12:41085302-41085352	HIPEpiC	eye:	n/a
23	chr12:41083590-41083640	HCM	heart:	n/a
24	chr12:41087520-41087570	PANC-1	pancreas:	n/a
25	chr12:41086282-41086332	AoSMC	blood vessel:	n/a
26	chr12:41086050-41086100	SK-N-SH_RA	brain:	n/a
27	chr12:40959011-40959061	HUVEC	blood vessel:	n/a
28	chr12:41086198-41086248	GM12878	blood:	n/a
29	chr12:41087520-41087570	IMR90	lung:	fetal
30	chr12:41086282-41086332	SKMC	muscle:	n/a
31	chr12:41087584-41087634	AG04450	lung:	fetal
32	chr12:41087092-41087142	Hepatocyte	liver:	n/a
33	chr12:41086277-41086327	HRPEpiC	eye:	n/a
34	chr12:41087584-41087634	SAEC	small airway:	n/a
35	chr12:41087252-41087302	HMEC	breast:	n/a
36	chr12:41086800-41086850	AoSMC	blood vessel:	n/a
37	chr12:41086198-41086248	T-47D	breast:	n/a
38	chr12:41087092-41087142	HNPCEpiC	eye:	n/a
39	chr12:41086050-41086100	HepG2	liver:	n/a
40	chr12:41043074-41043124	Hela-S3	cervix:	n/a
41	chr12:41086274-41086324	HIPEpiC	eye:	n/a
42	chr12:41043074-41043124	SK-N-SH	brain:	n/a
43	chr12:41087459-41087509	HCM	heart:	n/a
44	chr12:41086198-41086248	NT2-D1	testis:	n/a
45	chr12:41086274-41086324	BJ	skin:	n/a
46	chr12:41086680-41086730	HRE	kidney:	n/a
47	chr12:41085901-41085951	GM12878	blood:	n/a
48	chr12:41086282-41086332	K562	blood:	n/a
49	chr12:41085901-41085951	GM06990	blood:	n/a
50	chr12:41085286-41085336	HNPCEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:41015843..41016729-chr12:41315089..41315598,2	K562	blood:
2	chr12:41015662..41016670-chr12:41314832..41315906,5	MCF-7	breast:
3	chr12:41058052..41059920-chr12:41067347..41069015,2	K562	blood:
4	chr12:41018576..41021441-chr12:41028781..41031476,2	MCF-7	breast:
5	chr12:40974030..40975876-chr12:40978694..40980782,2	K562	blood:
6	chr12:41061679..41063997-chr12:41066307..41068227,2	K562	blood:
7	chr12:40974030..40975876-chr12:40978694..40980782,2	K562	blood:
8	chr12:41106289..41108607-chr12:41111961..41113819,2	K562	blood:
9	chr12:41061679..41063997-chr12:41066307..41068227,2	K562	blood:
10	chr12:41058052..41059920-chr12:41067347..41069015,2	K562	blood:
11	chr12:41018576..41021441-chr12:41028781..41031476,2	MCF-7	breast:
12	chr12:41106289..41108607-chr12:41111961..41113819,2	K562	blood:
13	chr12:41015832..41017042-chr12:41315031..41316480,11	MCF-7	breast:
14	chr12:40718883..40719693-chr12:40958776..40959283,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MUC19-1	chr12:40959435-40959597	NONHSAT027728
2	lnc-MUC19-1	chr12:40954806-40954856	NONHSAT027728
3	lnc-MUC19-1	chr12:40964265-40964562	NONHSAT027728
4	lnc-MUC19-1	chr12:40955364-40955411	NONHSAT027728
5	lnc-MUC19-1	chr12:40957333-40957362	NONHSAT027728
6	lnc-MUC19-1	chr12:40959928-40959965	NONHSAT027728
7	lnc-MUC19-1	chr12:40963498-40963606	NONHSAT027728
8	lnc-MUC19-1	chr12:40950947-40950997	NONHSAT027728
9	lnc-MUC19-1	chr12:40951266-40951319	NONHSAT027728
10	lnc-MUC19-1	chr12:40955141-40955194	NONHSAT027728
11	lnc-MUC19-1	chr12:40961400-40961514	NONHSAT027728
12	lnc-MUC19-1	chr12:40944483-40944536	NONHSAT027728
13	lnc-MUC19-1	chr12:40959315-40959346	NONHSAT027728
14	lnc-MUC19-1	chr12:40943907-40943960	NONHSAT027728
15	lnc-MUC19-1	chr12:40944284-40944337	NONHSAT027728
16	lnc-MUC19-1	chr12:40953037-40953090	NONHSAT027728
17	lnc-MUC19-1	chr12:40951895-40951936	NONHSAT027728
18	lnc-MUC19-3	chr12:41122613-41123699	NONHSAT027743
19	lnc-MUC19-1	chr12:40943698-40943751	NONHSAT027728
20	lnc-MUC19-1	chr12:40943399-40943446	NONHSAT027728
21	lnc-MUC19-1	chr12:40962809-40962844	NONHSAT027728
22	lnc-MUC19-1	chr12:40954338-40954391	NONHSAT027728

No data

Variant related genes	Relation type
ENSG00000257680	TF binding region
CNTN1	TF binding region
RNU6-713P	TF binding region
MUC19	TF binding region
ENSG00000257680	CpG island
CNTN1	CpG island
RNU6-713P	CpG island
MUC19	CpG island

Extended variants
information (count: 5281 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5281 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74469723	chr12:40943238-40943239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs561145095	chr12:40943243-40943244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555873372	chr12:40943258-40943259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574115463	chr12:40943272-40943273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1463738	chr12:40943329-40943330	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs371592421	chr12:40943416-40943417	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs200425036	chr12:40943451-40943452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578158930	chr12:40943452-40943453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34697723	chr12:40943456-40943457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190192242	chr12:40943463-40943464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563778260	chr12:40943519-40943520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531111605	chr12:40943556-40943557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11177168	chr12:40943609-40943610	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561412764	chr12:40943641-40943642	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528878442	chr12:40943643-40943644	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs557316288	chr12:40943709-40943710	Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs182055549	chr12:40943725-40943726	Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs80014625	chr12:40943730-40943731	Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs368354798	chr12:40943736-40943737	Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs186690841	chr12:40943749-40943750	Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs551648300	chr12:40943774-40943775	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569777030	chr12:40943798-40943799	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376281574	chr12:40943809-40943810	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191448173	chr12:40943810-40943811	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138444914	chr12:40943811-40943812	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs567716965	chr12:40943895-40943896	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150722934	chr12:40943952-40943953	Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs553136078	chr12:40943960-40943961	Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs1492316	chr12:40943970-40943971	Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs185550303	chr12:40943977-40943978	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535055229	chr12:40943985-40943986	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369376900	chr12:40944053-40944054	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557617609	chr12:40944074-40944075	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373387181	chr12:40944095-40944096	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1492315	chr12:40944102-40944103	Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs112695036	chr12:40944108-40944109	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199915268	chr12:40944124-40944125	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs561779556	chr12:40944135-40944136	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189178460	chr12:40944140-40944141	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540715244	chr12:40944146-40944147	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559131469	chr12:40944195-40944196	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs192877735	chr12:40944201-40944202	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs185359590	chr12:40944205-40944206	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs552927900	chr12:40944208-40944209	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs543773359	chr12:40944341-40944342	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs563563222	chr12:40944383-40944384	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs530745162	chr12:40944397-40944398	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs188555989	chr12:40944400-40944401	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs567461310	chr12:40944401-40944402	Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs528516753	chr12:40944456-40944457	Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Ewing''s sarcoma	19144156	CNVD

Chromatin state (count:627 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40936600-40943600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:40943400-40944600	Enhancers	HMEC	breast
3	chr12:40943600-40944600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:40944600-40945600	Weak transcription	HMEC	breast
5	chr12:40944600-40945800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:40945600-40947200	Enhancers	HMEC	breast
7	chr12:40947000-40947400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:40947400-40967800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:40948000-40948400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:40948400-40949000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:40948800-40949200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr12:40949000-40949600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr12:40949600-40951800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr12:40951800-40952200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr12:40952600-40954800	Enhancers	GM12878-XiMat	blood
16	chr12:40954800-40955800	Flanking Active TSS	GM12878-XiMat	blood
17	chr12:40955800-40956000	Enhancers	GM12878-XiMat	blood
18	chr12:40956000-40963600	Weak transcription	GM12878-XiMat	blood
19	chr12:40960200-40961200	Enhancers	A549	lung
20	chr12:40961400-40962200	Weak transcription	A549	lung
21	chr12:40962400-40962600	Weak transcription	A549	lung
22	chr12:40962800-40964400	Enhancers	A549	lung
23	chr12:40962800-40964600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:40963200-40964400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr12:40963200-40964400	Enhancers	NHDF-Ad	bronchial
26	chr12:40963200-40964800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:40963600-40963800	Enhancers	GM12878-XiMat	blood
28	chr12:40974200-40974400	ZNF genes & repeats	Pancreas	Pancrea
29	chr12:40977200-40977400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr12:40977400-40978000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:40978000-40979600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:40979600-40981200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr12:40980200-40980600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:40981200-40981800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr12:40982200-40984800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:40983600-40984200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr12:40984000-40984800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr12:40985400-40985600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr12:40985600-40986000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr12:40985600-40986400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:40986000-40986400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr12:40998000-40999800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr12:41001800-41008200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:41008000-41008800	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr12:41008000-41009000	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr12:41008000-41009600	Enhancers	GM12878-XiMat	blood
47	chr12:41008200-41008800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr12:41008200-41008800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr12:41008200-41009000	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr12:41008400-41009000	Enhancers	HMEC	breast

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