Variant report

Variant	esv3432683
Chromosome Location	chr12:10470734-10527581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1186)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10513720-10513857	K562	blood:	n/a	n/a
2	ARID3A	chr12:10519484-10519894	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:10515922-10516407	K562	blood:	n/a	n/a
4	ARID3A	chr12:10517306-10518105	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:10514385-10514386	K562	blood:	n/a	n/a
6	ATF1	chr12:10518006-10518279	K562	blood:	n/a	n/a
7	ATF1	chr12:10515987-10516344	K562	blood:	n/a	n/a
8	ATF1	chr12:10518698-10519024	K562	blood:	n/a	n/a
9	ATF2	chr12:10516736-10518064	GM12878	blood:	n/a	n/a
10	ATF2	chr12:10473155-10473759	GM12878	blood:	n/a	n/a
11	ATF2	chr12:10516513-10517982	GM12878	blood:	n/a	n/a
12	ATF2	chr12:10515391-10516378	GM12878	blood:	n/a	n/a
13	ATF2	chr12:10515378-10516482	GM12878	blood:	n/a	n/a
14	ATF2	chr12:10470709-10471203	GM12878	blood:	n/a	n/a
15	ATF2	chr12:10517765-10518225	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr12:10517788-10518192	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr12:10470741-10471136	GM12878	blood:	n/a	n/a
18	ATF3	chr12:10515933-10516347	K562	blood:	n/a	n/a
19	BACH1	chr12:10517085-10517124	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr12:10516901-10517786	GM12878	blood:	n/a	n/a
21	BATF	chr12:10473160-10473741	GM12878	blood:	n/a	n/a
22	BATF	chr12:10473434-10473653	GM12878	blood:	n/a	n/a
23	BATF	chr12:10473216-10473419	GM12878	blood:	n/a	n/a
24	BATF	chr12:10470851-10471221	GM12878	blood:	n/a	chr12:10471022-10471030
25	BCL11A	chr12:10516986-10517620	GM12878	blood:	n/a	n/a
26	BCL11A	chr12:10473293-10473615	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:10517007-10517370	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:10515491-10515913	GM12878	blood:	n/a	n/a
29	BCL3	chr12:10515498-10515948	GM12878	blood:	n/a	n/a
30	BCL3	chr12:10470815-10471173	GM12878	blood:	n/a	chr12:10470997-10471006
31	BCLAF1	chr12:10516330-10516752	GM12878	blood:	n/a	n/a
32	BCLAF1	chr12:10473313-10473710	GM12878	blood:	n/a	n/a
33	BCLAF1	chr12:10470778-10471247	GM12878	blood:	n/a	chr12:10470997-10471006
34	BCLAF1	chr12:10516740-10517803	GM12878	blood:	n/a	n/a
35	BCLAF1	chr12:10516769-10517765	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:10516861-10517974	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:10515999-10516244	K562	blood:	n/a	n/a
38	BHLHE40	chr12:10516495-10517792	K562	blood:	n/a	n/a
39	BHLHE40	chr12:10484273-10484556	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:10515601-10515915	GM12878	blood:	n/a	n/a
41	BHLHE40	chr12:10472918-10473181	GM12878	blood:	n/a	n/a
42	BRCA1	chr12:10507323-10507343	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr12:10517548-10518007	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr12:10515912-10516253	K562	blood:	n/a	n/a
45	CBX3	chr12:10510572-10510765	K562	blood:	n/a	n/a
46	CEBPB	chr12:10515912-10516396	K562	blood:	n/a	n/a
47	CEBPB	chr12:10515495-10517606	GM12878	blood:	n/a	n/a
48	CEBPB	chr12:10474613-10474641	HepG2	liver:	n/a	n/a
49	CEBPB	chr12:10487581-10487803	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:10517435-10518128	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10516240-10516290	SKMC	muscle:	n/a
2	chr12:10515574-10515624	AG10803	skin:	n/a
3	chr12:10516240-10516290	HUVEC	blood vessel:	n/a
4	chr12:10515574-10515624	IMR90	lung:	fetal
5	chr12:10525233-10525283	HCM	heart:	n/a
6	chr12:10515091-10515141	GM19239	blood:	n/a
7	chr12:10516240-10516290	IMR90	lung:	fetal
8	chr12:10516240-10516290	BE2_C	brain:	n/a
9	chr12:10515091-10515141	ECC-1	luminal epithelium:	n/a
10	chr12:10515574-10515624	SK-N-MC	brain:	n/a
11	chr12:10525233-10525283	HepG2	liver:	n/a
12	chr12:10525233-10525283	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:10525233-10525283	HRCEpiC	kidney:	n/a
14	chr12:10525233-10525283	SKMC	muscle:	n/a
15	chr12:10516240-10516290	ovcar-3	ovarian:	n/a
16	chr12:10525233-10525283	GM06990	blood:	n/a
17	chr12:10525233-10525283	SAEC	small airway:	n/a
18	chr12:10516240-10516290	HNPCEpiC	eye:	n/a
19	chr12:10515574-10515624	K562	blood:	n/a
20	chr12:10525233-10525283	Caco-2	colon:	n/a
21	chr12:10515574-10515624	Caco-2	colon:	n/a
22	chr12:10515091-10515141	HRPEpiC	eye:	n/a
23	chr12:10515091-10515141	NT2-D1	testis:	n/a
24	chr12:10525233-10525283	Hepatocyte	liver:	n/a
25	chr12:10525233-10525283	MCF-7	breast:	n/a
26	chr12:10515574-10515624	HCF	heart:	n/a
27	chr12:10515574-10515624	HRE	kidney:	n/a
28	chr12:10515574-10515624	BJ	skin:	n/a
29	chr12:10515574-10515624	H1-hESC	embryonic stem cell:	embryo
30	chr12:10515574-10515624	ProgFib	skin:	n/a
31	chr12:10516240-10516290	PFSK-1	brain:	n/a
32	chr12:10515574-10515624	GM06990	blood:	n/a
33	chr12:10516240-10516290	SK-N-SH	brain:	n/a
34	chr12:10525233-10525283	GM19239	blood:	n/a
35	chr12:10515091-10515141	U87	brain:	n/a
36	chr12:10515574-10515624	GM12878	blood:	n/a
37	chr12:10515091-10515141	PANC-1	pancreas:	n/a
38	chr12:10525233-10525283	NHBE	bronchial:	n/a
39	chr12:10525233-10525283	NB4	blood:	n/a
40	chr12:10525233-10525283	HEEpiC	esophagus:	n/a
41	chr12:10515091-10515141	SK-N-SH_RA	brain:	n/a
42	chr12:10515574-10515624	A549	lung:	n/a
43	chr12:10515091-10515141	GM12878	blood:	n/a
44	chr12:10515574-10515624	MCF-7	breast:	n/a
45	chr12:10515091-10515141	SK-N-MC	brain:	n/a
46	chr12:10516240-10516290	SK-N-MC	brain:	n/a
47	chr12:10525233-10525283	CMK	blood:	n/a
48	chr12:10515574-10515624	AG09319	gingival:	n/a
49	chr12:10525233-10525283	Jurkat	blood:	n/a
50	chr12:10515091-10515141	AG04449	skin:	fetal

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:10518506..10519182-chr16:20688297..20688797,2	HCT-116	colon:
2	chr12:10436832..10439225-chr12:10509141..10511407,2	K562	blood:
3	chr12:10506746..10508549-chr12:10514255..10516412,2	K562	blood:
4	chr12:10515701..10517485-chr12:10526352..10529351,3	K562	blood:
5	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
6	chr12:10484283..10485072-chr12:10714510..10715568,4	K562	blood:
7	chr12:10520202..10521817-chr12:10526312..10528193,2	K562	blood:
8	chr12:10515701..10519228-chr12:10526352..10529377,4	K562	blood:
9	chr12:10483978..10484906-chr12:10714545..10715159,3	MCF-7	breast:
10	chr12:10484044..10484911-chr12:10711156..10712037,3	MCF-7	breast:
11	chr12:10509675..10512643-chr12:10514341..10517366,3	K562	blood:
12	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
13	chr12:10483953..10484953-chr12:10826469..10827411,2	K562	blood:
14	chr12:10470749..10472594-chr12:10475991..10477834,2	K562	blood:
15	chr12:10484099..10484956-chr12:10652861..10653779,2	MCF-7	breast:
16	chr12:10519323..10520144-chr12:10902384..10903013,2	MCF-7	breast:
17	chr12:10484518..10485026-chr12:10826902..10827419,2	MCF-7	breast:
18	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
19	chr12:10507526..10509637-chr12:10511583..10513205,2	K562	blood:
20	chr12:10484385..10484963-chr12:10714626..10715246,2	MCF-7	breast:
21	chr12:10527378..10530229-chr12:10546803..10548399,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-277P12.7.1-2	chr12:10490644-10490891	ENSG00000256288
2	lnc-RP11-277P12.7.1-1	chr12:10511063-10511162	ENSG00000256155
3	lnc-RP11-277P12.7.1-2	chr12:10488711-10488908	ENSG00000256288
4	lnc-RP11-277P12.7.1-2	chr12:10485460-10485662	ENSG00000256288
5	lnc-RP11-277P12.7.1-1	chr12:10513183-10513644	ENSG00000256155
6	lnc-KLRD1-1	chr12:10526634-10526735	ENSG00000245648
7	lnc-KLRD1-1	chr12:10516368-10516632	ENSG00000245648

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KLRK1	hsa-miR-9-5p	chr12:10525600-10525624

Variant related genes	Relation type
ENSG00000256288	TF binding region
ENSG00000245648	TF binding region
ENSG00000256155	TF binding region
ENSG00000256288	CpG island
ENSG00000245648	CpG island
ENSG00000256155	CpG island
ENSG00000245648	chromatin interactions
ENSG00000256888	chromatin interactions
ENSG00000060140	chromatin interactions
RNF111	miRNA target sites
SMAD4	miRNA target sites
LPHN2	miRNA target sites
NFIB	miRNA target sites
KIAA1967	miRNA target sites

Extended variants
information (count: 2761 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2761 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560932405	chr12:10470773-10470774	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534526027	chr12:10470853-10470854	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs543271843	chr12:10470891-10470892	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563082136	chr12:10470930-10470931	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531953302	chr12:10470936-10470937	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145640011	chr12:10470956-10470957	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148473837	chr12:10470963-10470964	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527637219	chr12:10470987-10470988	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12303914	chr12:10471050-10471051	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
10	rs79017632	chr12:10471075-10471076	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530110682	chr12:10471112-10471113	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549752303	chr12:10471114-10471115	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112343486	chr12:10471155-10471156	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71434128	chr12:10471162-10471163	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538560930	chr12:10471170-10471171	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147610442	chr12:10471172-10471173	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552736850	chr12:10471179-10471180	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565695891	chr12:10471226-10471227	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534573072	chr12:10471227-10471228	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554583590	chr12:10471259-10471260	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574619897	chr12:10471272-10471273	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543534130	chr12:10471278-10471279	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560780557	chr12:10471306-10471307	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12813197	chr12:10471317-10471318	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs564547750	chr12:10471337-10471338	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113561161	chr12:10471338-10471339	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112462536	chr12:10471342-10471343	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545385697	chr12:10471376-10471377	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113059173	chr12:10471377-10471378	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200087863	chr12:10471399-10471400	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541052707	chr12:10471439-10471440	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75637382	chr12:10471443-10471444	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11374003	chr12:10471445-10471446	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs75662061	chr12:10471447-10471448	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560929191	chr12:10471484-10471485	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530183322	chr12:10471491-10471492	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188452491	chr12:10471579-10471580	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs569762421	chr12:10471607-10471608	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs114195530	chr12:10471609-10471610	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs533509911	chr12:10471613-10471614	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs369304293	chr12:10471661-10471662	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs76386506	chr12:10471665-10471666	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs111824819	chr12:10471693-10471694	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs141603548	chr12:10471756-10471757	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs534899978	chr12:10471780-10471781	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs554645474	chr12:10471792-10471793	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs568060101	chr12:10471794-10471795	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs536748405	chr12:10471905-10471906	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs147892854	chr12:10471966-10471967	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs576574555	chr12:10471975-10471976	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1287 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10454800-10474400	Weak transcription	Left Ventricle	heart
2	chr12:10462800-10471400	Weak transcription	Right Ventricle	heart
3	chr12:10463200-10470800	Weak transcription	Placenta	Placenta
4	chr12:10467400-10472600	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr12:10469400-10476600	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr12:10470800-10472400	Strong transcription	Placenta	Placenta
7	chr12:10471600-10472400	ZNF genes & repeats	GM12878-XiMat	blood
8	chr12:10472400-10473200	Weak transcription	GM12878-XiMat	blood
9	chr12:10472400-10474000	Weak transcription	Placenta	Placenta
10	chr12:10472600-10474200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:10473000-10474000	Enhancers	Primary T cells from cord blood	blood
12	chr12:10473200-10474000	Enhancers	GM12878-XiMat	blood
13	chr12:10473200-10474600	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr12:10473400-10473800	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr12:10474200-10474800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr12:10474800-10475400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr12:10475400-10476400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr12:10476400-10476800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr12:10476600-10476800	Enhancers	Primary T cells fromperipheralblood	blood
20	chr12:10476800-10482600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:10478400-10483800	Weak transcription	Right Ventricle	heart
22	chr12:10479400-10479800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr12:10480200-10480400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr12:10480400-10488800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr12:10482600-10483000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr12:10483000-10484200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:10483000-10485400	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr12:10483800-10484200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:10483800-10485600	Enhancers	Hela-S3	cervix
30	chr12:10484000-10485000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr12:10484200-10484400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:10484200-10484400	Enhancers	Brain Angular Gyrus	brain
33	chr12:10484200-10484600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr12:10484200-10491800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr12:10484400-10484800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:10485400-10485600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr12:10485600-10488000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr12:10487800-10488200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr12:10488000-10491400	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr12:10488200-10488600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:10488400-10489400	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr12:10488600-10489000	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr12:10488600-10489400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:10488600-10489600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr12:10488800-10489000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr12:10489000-10489600	Active TSS	H9 Cell Line	embryonic stem cell
47	chr12:10489000-10490200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr12:10489400-10489600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr12:10489400-10490400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr12:10489400-10491400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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