Variant report

Variant	esv2557795
Chromosome Location	chr12:8533001-8596370
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	BACH1	chr12:8549275-8549403	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr12:8572227-8572466	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:8543218-8543226	GM12878	blood:	n/a	n/a
4	BHLHE40	chr12:8549365-8549435	GM12878	blood:	n/a	n/a
5	CEBPB	chr12:8550591-8550718	IMR90	lung:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
6	CEBPB	chr12:8550579-8550720	HepG2	liver:	n/a	chr12:8550656-8550665 chr12:8550654-8550665 chr12:8550654-8550667
7	CHD2	chr12:8543173-8543243	GM12878	blood:	n/a	n/a
8	CTCF	chr12:8549340-8549490	GM12870	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
9	CTCF	chr12:8591390-8591459	GM10248	blood:	n/a	n/a
10	CTCF	chr12:8543132-8543416	GM13976	blood:	n/a	n/a
11	CTCF	chr12:8549360-8549510	AG09319	gingival:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
12	CTCF	chr12:8543180-8543330	HVMF	connective:	n/a	n/a
13	CTCF	chr12:8543220-8543370	GM12867	blood:	n/a	n/a
14	CTCF	chr12:8543212-8543355	K562	blood:	n/a	n/a
15	CTCF	chr12:8549360-8549510	A549	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
16	CTCF	chr12:8543180-8543330	HFF	foreskin:	n/a	n/a
17	CTCF	chr12:8543240-8543390	MCF-7	breast:	n/a	n/a
18	CTCF	chr12:8543109-8543433	Spleen_OC	spleen:	n/a	n/a
19	CTCF	chr12:8549320-8549470	AG09309	skin:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
20	CTCF	chr12:8543220-8543370	Caco-2	colon:	n/a	n/a
21	CTCF	chr12:8549360-8549510	HAc	cerebellar:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
22	CTCF	chr12:8549312-8549539	HUVEC	blood vessel:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
23	CTCF	chr12:8543114-8543426	NHEK	skin:	n/a	n/a
24	CTCF	chr12:8549360-8549510	GM12871	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
25	CTCF	chr12:8549360-8549510	BE2_C	brain:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
26	CTCF	chr12:8543220-8543370	NHEK	skin:	n/a	n/a
27	CTCF	chr12:8543180-8543330	AG04450	lung:	n/a	n/a
28	CTCF	chr12:8549380-8549530	HPAF	blood vessel:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
29	CTCF	chr12:8543200-8543350	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr12:8543145-8543389	GM10248	blood:	n/a	n/a
31	CTCF	chr12:8543176-8543350	Medullo	brain:	n/a	n/a
32	CTCF	chr12:8543180-8543330	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr12:8549271-8549529	ECC-1	luminal epithelium:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
34	CTCF	chr12:8549297-8549581	GM13976	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
35	CTCF	chr12:8549320-8549470	HepG2	liver:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
36	CTCF	chr12:8549205-8549541	A549	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
37	CTCF	chr12:8549460-8549610	GM06990	blood:	n/a	n/a
38	CTCF	chr12:8543180-8543330	RPTEC	kidney:	n/a	n/a
39	CTCF	chr12:8594350-8594390	LNCaP	prostate:	n/a	n/a
40	CTCF	chr12:8543005-8543439	K562	blood:	n/a	n/a
41	CTCF	chr12:8549360-8549510	NHLF	lung:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
42	CTCF	chr12:8549320-8549470	SK-N-SH_RA	brain:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
43	CTCF	chr12:8543220-8543370	GM12873	blood:	n/a	n/a
44	CTCF	chr12:8549360-8549510	GM12864	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414
45	CTCF	chr12:8543191-8543402	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr12:8543200-8543350	RPTEC	kidney:	n/a	n/a
47	CTCF	chr12:8543220-8543370	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr12:8549621-8549780	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr12:8543098-8543388	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr12:8549262-8549599	GM19240	blood:	n/a	chr12:8549394-8549415 chr12:8549399-8549417 chr12:8549401-8549414 chr12:8549400-8549416 chr12:8549401-8549414

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8542756-8542806	Hepatocyte	liver:	n/a
2	chr12:8542756-8542806	Hepatocyte	liver:	n/a
3	chr12:8549511-8549561	T-47D	breast:	n/a
4	chr12:8557855-8557905	HCT-116	colon:	n/a
5	chr12:8562937-8562987	HPAEpiC	pulmonary alveolar:	n/a
6	chr12:8575139-8575189	HEK293	kidney:	embryo
7	chr12:8570210-8570260	GM06990	blood:	n/a
8	chr12:8541476-8541526	NHDF-neo	bronchial:	n/a
9	chr12:8543333-8543383	AG04449	skin:	fetal
10	chr12:8576728-8576778	HRCEpiC	kidney:	n/a
11	chr12:8596320-8596370	HMEC	breast:	n/a
12	chr12:8571692-8571742	BE2_C	brain:	n/a
13	chr12:8549243-8549293	AG10803	skin:	n/a
14	chr12:8575691-8575741	HEK293	kidney:	embryo
15	chr12:8549446-8549496	Jurkat	blood:	n/a
16	chr12:8549243-8549293	AG04449	skin:	fetal
17	chr12:8570268-8570318	HepG2	liver:	n/a
18	chr12:8548923-8548973	K562	blood:	n/a
19	chr12:8559628-8559678	SK-N-MC	brain:	n/a
20	chr12:8575691-8575741	HRCEpiC	kidney:	n/a
21	chr12:8562937-8562987	HUVEC	blood vessel:	n/a
22	chr12:8557855-8557905	HEEpiC	esophagus:	n/a
23	chr12:8544796-8544846	K562	blood:	n/a
24	chr12:8539716-8539766	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:8542524-8542574	SK-N-SH_RA	brain:	n/a
26	chr12:8549457-8549507	NHDF-neo	bronchial:	n/a
27	chr12:8548978-8549028	HepG2	liver:	n/a
28	chr12:8542524-8542574	HPAEpiC	pulmonary alveolar:	n/a
29	chr12:8543302-8543352	NT2-D1	testis:	n/a
30	chr12:8542756-8542806	ovcar-3	ovarian:	n/a
31	chr12:8559628-8559678	NH-A	brain:	n/a
32	chr12:8549446-8549496	ECC-1	luminal epithelium:	n/a
33	chr12:8548978-8549028	HL-60	blood:	n/a
34	chr12:8551501-8551551	HRPEpiC	eye:	n/a
35	chr12:8549446-8549496	K562	blood:	n/a
36	chr12:8548923-8548973	SK-N-MC	brain:	n/a
37	chr12:8544796-8544846	GM12878	blood:	n/a
38	chr12:8549243-8549293	GM19239	blood:	n/a
39	chr12:8548978-8549028	K562	blood:	n/a
40	chr12:8576728-8576778	GM12892	blood:	n/a
41	chr12:8576728-8576778	RPTEC	kidney:	n/a
42	chr12:8570210-8570260	HEK293	kidney:	embryo
43	chr12:8542524-8542574	HCPEpiC	choroid plexus:	n/a
44	chr12:8575139-8575189	ProgFib	skin:	n/a
45	chr12:8548978-8549028	NHDF-neo	bronchial:	n/a
46	chr12:8544796-8544846	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:8562937-8562987	PANC-1	pancreas:	n/a
48	chr12:8549446-8549496	PFSK-1	brain:	n/a
49	chr12:8542839-8542889	PFSK-1	brain:	n/a
50	chr12:8575139-8575189	SK-N-SH	brain:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC4E-2	chr12:8542866-8543107	ENSG00000226091.2
2	lnc-CLEC4E-2	chr12:8542866-8543107	NONHSAT026335
3	lnc-CLEC4E-2	chr12:8538284-8538442	ENSG00000226091.2
4	lnc-CLEC4E-2	chr12:8542866-8543398	NONHSAT026332
5	lnc-CLEC4E-2	chr12:8535440-8535671	ENSG00000226091.2
6	lnc-CLEC4E-2	chr12:8539359-8540500	ENSG00000226091.2
7	lnc-CLEC4E-2	chr12:8536701-8537017	ENSG00000226091.2
8	lnc-CLEC4E-2	chr12:8537740-8537895	ENSG00000226091.2
9	lnc-CLEC4E-2	chr12:8549019-8549091	ENSG00000226091.2
10	lnc-CLEC4E-2	chr12:8549019-8549212	NONHSAT026335
11	lnc-CLEC4E-2	chr12:8542866-8543348	NR_024420
12	lnc-CLEC4E-2	chr12:8538284-8538323	ENSG00000226091.2
13	lnc-CLEC4E-2	chr12:8542866-8543348	ENSG00000226091.2
14	lnc-CLEC4E-2	chr12:8543498-8543565	ENSG00000226091.2
15	lnc-CLEC4E-2	chr12:8542883-8542933	ENSG00000226091.2

Variant related genes	Relation type
OR7E140P	TF binding region
ENSG00000266218	TF binding region
LINC00937	TF binding region
OR7E148P	TF binding region
ENSG00000256136	TF binding region
OR7E149P	TF binding region
OR7E140P	CpG island
ENSG00000266218	CpG island
LINC00937	CpG island
OR7E148P	CpG island
ENSG00000256136	CpG island
OR7E149P	CpG island

Extended variants
information (count: 1209 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1209 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12298634	chr12:8533016-8533017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs71042381	chr12:8533045-8533046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374148777	chr12:8533059-8533060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189419517	chr12:8533060-8533061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12313826	chr12:8533110-8533111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12299994	chr12:8533116-8533117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181527626	chr12:8533119-8533120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538855430	chr12:8533127-8533128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71042382	chr12:8533129-8533130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12830396	chr12:8533130-8533131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12830402	chr12:8533136-8533137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs57103608	chr12:8533162-8533163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113293835	chr12:8533171-8533172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150018372	chr12:8533175-8533176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75678683	chr12:8533223-8533224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77838167	chr12:8533227-8533228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185330376	chr12:8533235-8533236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76147563	chr12:8533238-8533239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146570381	chr12:8533250-8533251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189375539	chr12:8533276-8533277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11044982	chr12:8533282-8533283	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181584112	chr12:8533292-8533293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370012309	chr12:8533379-8533380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12427341	chr12:8533413-8533414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185910189	chr12:8533414-8533415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537848168	chr12:8533420-8533421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371008336	chr12:8533437-8533438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376261131	chr12:8533455-8533456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189976019	chr12:8533483-8533484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146880521	chr12:8533510-8533511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181847629	chr12:8533535-8533536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554496898	chr12:8533548-8533549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574504749	chr12:8533565-8533566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186340971	chr12:8533645-8533646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115071759	chr12:8533664-8533665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11044983	chr12:8533666-8533667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7974369	chr12:8533690-8533691	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577347228	chr12:8533702-8533703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191094396	chr12:8533719-8533720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183255688	chr12:8533793-8533794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188847647	chr12:8533811-8533812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35525911	chr12:8533980-8533981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564824008	chr12:8533982-8533983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs397850084	chr12:8533991-8533992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181891715	chr12:8534018-8534019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12831093	chr12:8534040-8534041	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs191145697	chr12:8534068-8534069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9705441	chr12:8534119-8534120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115011847	chr12:8534121-8534122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12831152	chr12:8534123-8534124	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
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
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8527200-8542600	Weak transcription	Right Atrium	heart
2	chr12:8531600-8533600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr12:8531600-8537400	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr12:8532400-8533600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:8533600-8533800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr12:8533600-8533800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:8533800-8534400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:8534400-8535000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:8535000-8541600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr12:8535000-8542000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:8535400-8541600	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr12:8537400-8537800	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr12:8537400-8538200	Enhancers	HUVEC	blood vessel
14	chr12:8537800-8542000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:8541200-8542000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr12:8541600-8542000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr12:8541800-8542000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
18	chr12:8542000-8542200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr12:8542000-8542200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr12:8542000-8542200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr12:8542000-8542200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
22	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
23	chr12:8542000-8542200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
26	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr12:8542000-8542200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
28	chr12:8542000-8542200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
29	chr12:8542000-8542200	Enhancers	Esophagus	oesophagus
30	chr12:8542000-8542200	Enhancers	Pancreas	Pancrea
31	chr12:8542000-8542200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
32	chr12:8542000-8542400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
33	chr12:8542000-8542400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:8542000-8542400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:8542000-8542400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr12:8542000-8542400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
37	chr12:8542000-8542600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr12:8542000-8542600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
39	chr12:8542000-8542600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:8542000-8542600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr12:8542000-8542600	Bivalent Enhancer	Adipose Nuclei	Adipose
42	chr12:8542000-8542600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr12:8542000-8543200	Active TSS	iPS-15b Cell Line	embryonic stem cell
44	chr12:8542000-8543200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr12:8542200-8542400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr12:8542200-8542400	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
47	chr12:8542200-8542600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:8542200-8542600	Weak transcription	Pancreas	Pancrea
49	chr12:8542200-8542800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
50	chr12:8542200-8542800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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