Variant report

Variant	nsv916519
Chromosome Location	chr12:21017673-21356568
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	chr12:21322799-21322999	K562	blood:	n/a	n/a
2	BACH1	chr12:21350777-21350898	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:21090344-21090547	GM12878	blood:	n/a	n/a
4	BATF	chr12:21021928-21022137	GM12878	blood:	n/a	chr12:21022019-21022030
5	BHLHE40	chr12:21138511-21138625	GM12878	blood:	n/a	n/a
6	BRCA1	chr12:21322801-21323167	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr12:21308670-21308879	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr12:21103222-21103500	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:21193579-21193868	A549	lung:	n/a	chr12:21193754-21193765
10	CEBPB	chr12:21114301-21114316	A549	lung:	n/a	n/a
11	CEBPB	chr12:21215636-21215960	A549	lung:	n/a	n/a
12	CEBPB	chr12:21243014-21243312	A549	lung:	n/a	chr12:21243166-21243177
13	CEBPB	chr12:21297827-21298053	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:21036155-21036832	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
15	CEBPB	chr12:21193602-21193866	HepG2	liver:	n/a	chr12:21193754-21193765
16	CEBPB	chr12:21246783-21246933	HepG2	liver:	n/a	chr12:21246828-21246839
17	CEBPB	chr12:21071557-21071721	A549	lung:	n/a	n/a
18	CEBPB	chr12:21260031-21260260	IMR90	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
19	CEBPB	chr12:21168771-21169100	A549	lung:	n/a	chr12:21168919-21168930
20	CEBPB	chr12:21260029-21260209	A549	lung:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
21	CEBPB	chr12:21038089-21038427	A549	lung:	n/a	n/a
22	CEBPB	chr12:21325090-21325330	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr12:21036268-21036667	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
24	CEBPB	chr12:21037942-21038507	A549	lung:	n/a	n/a
25	CEBPB	chr12:21260027-21260258	HepG2	liver:	n/a	chr12:21260128-21260137 chr12:21260126-21260137 chr12:21260126-21260139
26	CEBPB	chr12:21056070-21056238	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:21234037-21234356	A549	lung:	n/a	chr12:21234179-21234190
28	CEBPB	chr12:21234009-21234357	HepG2	liver:	n/a	chr12:21234179-21234190
29	CEBPB	chr12:21168858-21169067	H1-hESC	embryonic stem cell:	n/a	chr12:21168919-21168930
30	CEBPB	chr12:21168774-21169104	HepG2	liver:	n/a	chr12:21168919-21168930
31	CEBPB	chr12:21233354-21233510	A549	lung:	n/a	n/a
32	CEBPB	chr12:21193722-21193901	H1-hESC	embryonic stem cell:	n/a	chr12:21193754-21193765
33	CEBPB	chr12:21175943-21176096	H1-hESC	embryonic stem cell:	n/a	chr12:21176036-21176047 chr12:21176037-21176048 chr12:21176036-21176049 chr12:21176038-21176047
34	CEBPB	chr12:21282343-21282678	HepG2	liver:	n/a	chr12:21282598-21282609 chr12:21282528-21282539
35	CEBPB	chr12:21038060-21038439	A549	lung:	n/a	n/a
36	CEBPB	chr12:21036282-21036646	Hela-S3	cervix:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
37	CEBPB	chr12:21234048-21234229	H1-hESC	embryonic stem cell:	n/a	chr12:21234179-21234190
38	CEBPB	chr12:21271000-21271136	HepG2	liver:	n/a	chr12:21271080-21271091
39	CEBPB	chr12:21243024-21243307	HepG2	liver:	n/a	chr12:21243166-21243177
40	CEBPB	chr12:21127431-21127656	HepG2	liver:	n/a	chr12:21127518-21127529
41	CEBPB	chr12:21133477-21133530	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:21036286-21036659	A549	lung:	n/a	chr12:21036463-21036474 chr12:21036307-21036318
43	CEBPB	chr12:21036323-21036549	HepG2	liver:	n/a	chr12:21036463-21036474
44	CEBPB	chr12:21243036-21243304	IMR90	lung:	n/a	chr12:21243166-21243177
45	CEBPB	chr12:21356519-21356864	IMR90	lung:	n/a	chr12:21356695-21356706
46	CEBPB	chr12:21065012-21065124	HepG2	liver:	n/a	chr12:21065034-21065045
47	CEBPB	chr12:21193668-21193806	K562	blood:	n/a	chr12:21193754-21193765
48	CEBPB	chr12:21175930-21176170	HepG2	liver:	n/a	chr12:21176036-21176047 chr12:21176037-21176048 chr12:21176036-21176049 chr12:21176038-21176047
49	CEBPB	chr12:21193668-21193868	Hela-S3	cervix:	n/a	chr12:21193754-21193765
50	CHD2	chr12:21218752-21218883	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:21283725-21283775	K562	blood:	n/a
2	chr12:21283725-21283775	NB4	blood:	n/a
3	chr12:21324585-21324635	NH-A	brain:	n/a
4	chr12:21287375-21287425	HPAEpiC	pulmonary alveolar:	n/a
5	chr12:21287375-21287425	T-47D	breast:	n/a
6	chr12:21283725-21283775	GM12878	blood:	n/a
7	chr12:21283725-21283775	PrEC	prostate:	n/a
8	chr12:21283725-21283775	HEK293	kidney:	embryo
9	chr12:21283725-21283775	SAEC	small airway:	n/a
10	chr12:21324585-21324635	HIPEpiC	eye:	n/a
11	chr12:21283725-21283775	HUVEC	blood vessel:	n/a
12	chr12:21324585-21324635	T-47D	breast:	n/a
13	chr12:21287375-21287425	NT2-D1	testis:	n/a
14	chr12:21287375-21287425	GM06990	blood:	n/a
15	chr12:21324585-21324635	HCT-116	colon:	n/a
16	chr12:21283725-21283775	CMK	blood:	n/a
17	chr12:21324585-21324635	LNCaP	prostate:	n/a
18	chr12:21287375-21287425	HIPEpiC	eye:	n/a
19	chr12:21283725-21283775	SKMC	muscle:	n/a
20	chr12:21283725-21283775	GM12892	blood:	n/a
21	chr12:21287375-21287425	GM12878	blood:	n/a
22	chr12:21287375-21287425	HAEpiC	amniotic membrane:	n/a
23	chr12:21324585-21324635	PFSK-1	brain:	n/a
24	chr12:21283725-21283775	NHBE	bronchial:	n/a
25	chr12:21287375-21287425	Hela-S3	cervix:	n/a
26	chr12:21324585-21324635	NB4	blood:	n/a
27	chr12:21324585-21324635	ECC-1	luminal epithelium:	n/a
28	chr12:21287375-21287425	ECC-1	luminal epithelium:	n/a
29	chr12:21283725-21283775	BJ	skin:	n/a
30	chr12:21324585-21324635	HepG2	liver:	n/a
31	chr12:21324585-21324635	MCF10A-Er-Src	breast:	n/a
32	chr12:21283725-21283775	HPAEpiC	pulmonary alveolar:	n/a
33	chr12:21287375-21287425	NHBE	bronchial:	n/a
34	chr12:21287375-21287425	U87	brain:	n/a
35	chr12:21287375-21287425	HepG2	liver:	n/a
36	chr12:21287375-21287425	SAEC	small airway:	n/a
37	chr12:21324585-21324635	U87	brain:	n/a
38	chr12:21283725-21283775	SK-N-SH_RA	brain:	n/a
39	chr12:21324585-21324635	NHBE	bronchial:	n/a
40	chr12:21324585-21324635	AG09319	gingival:	n/a
41	chr12:21283725-21283775	AG09319	gingival:	n/a
42	chr12:21283725-21283775	AG04449	skin:	fetal
43	chr12:21283725-21283775	NT2-D1	testis:	n/a
44	chr12:21283725-21283775	NHDF-neo	bronchial:	n/a
45	chr12:21287375-21287425	BE2_C	brain:	n/a
46	chr12:21287375-21287425	HRCEpiC	kidney:	n/a
47	chr12:21283725-21283775	AoSMC	blood vessel:	n/a
48	chr12:21324585-21324635	GM19239	blood:	n/a
49	chr12:21283725-21283775	HRCEpiC	kidney:	n/a
50	chr12:21324585-21324635	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
2	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:
3	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
4	chr12:21193958..21195458-chr17:59872939..59874521,2	MCF-7	breast:
5	chr12:21099420..21100309-chr12:21218592..21219170,2	MCF-7	breast:
6	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:
7	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:
8	chr12:21254641..21256921-chr12:21258871..21260640,2	K562	blood:
9	chr12:21154478..21155199-chr12:21322720..21323314,2	MCF-7	breast:
10	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
11	chr12:21102918..21103853-chr12:21322562..21323307,3	MCF-7	breast:
12	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
13	chr12:21154478..21155199-chr12:21322720..21323314,2	MCF-7	breast:
14	chr12:21099355..21100332-chr12:21322634..21323175,3	MCF-7	breast:
15	chr12:21099378..21100255-chr12:21322524..21323110,2	MCF-7	breast:
16	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
17	chr12:21354085..21355966-chr12:21358587..21360653,2	K562	blood:
18	chr12:21268556..21269333-chr7:84915114..84915941,2	MCF-7	breast:
19	chr12:21220478..21221206-chr12:21228660..21229307,2	MCF-7	breast:
20	chr12:21337800..21339752-chr12:21340612..21342590,2	K562	blood:
21	chr12:21103010..21104123-chr12:21218514..21219449,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1A2-5	chr12:21083248-21084757	NONHSAT027238
2	lnc-SLCO1B1-1	chr12:21228194-21228718	NONHSAT027240
3	lnc-SLCO1B1-1	chr12:21220285-21220317	NONHSAT027240

Variant related genes	Relation type
ENSG00000257062	TF binding region
SLCO1B1	TF binding region
SLCO1B7	TF binding region
ENSG00000257062	CpG island
SLCO1B1	CpG island
SLCO1B7	CpG island

Extended variants
information (count: 10247 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:10247 , 50 per page) page: 1 2 3 4 5 6 7 ... 205

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77854652	chr12:21017679-21017680	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115673184	chr12:21017680-21017681	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138178122	chr12:21017681-21017682	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556126887	chr12:21017696-21017697	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567139990	chr12:21017747-21017748	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2417941	chr12:21017796-21017797	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs534949077	chr12:21017850-21017851	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369880194	chr12:21017864-21017865	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs77041891	chr12:21017870-21017871	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2417940	chr12:21017875-21017876	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
11	rs142754510	chr12:21017888-21017889	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543856552	chr12:21017893-21017894	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563545654	chr12:21017954-21017955	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs80133659	chr12:21017975-21017976	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73069234	chr12:21018027-21018028	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs538399092	chr12:21018033-21018034	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76880107	chr12:21018046-21018047	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146075261	chr12:21018061-21018062	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148319004	chr12:21018071-21018072	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568716723	chr12:21018078-21018079	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577175564	chr12:21018128-21018129	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1991849	chr12:21018131-21018132	Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs12304440	chr12:21018139-21018140	Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs563216786	chr12:21018156-21018157	Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187818501	chr12:21018280-21018281	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs193223082	chr12:21018299-21018300	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs9739022	chr12:21018305-21018306	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546405419	chr12:21018307-21018308	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529070574	chr12:21018393-21018394	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566424208	chr12:21018401-21018402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7138198	chr12:21018402-21018403	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs559479646	chr12:21018414-21018415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540115512	chr12:21018427-21018428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7138316	chr12:21018467-21018468	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs59996209	chr12:21018517-21018518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374929442	chr12:21018536-21018537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557058408	chr12:21018607-21018608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150869097	chr12:21018690-21018691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183777372	chr12:21018757-21018758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188787149	chr12:21018775-21018776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559318069	chr12:21018789-21018790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7138939	chr12:21018802-21018803	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs7309891	chr12:21018855-21018856	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs201441393	chr12:21018917-21018918	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533180508	chr12:21018931-21018932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549696707	chr12:21018933-21018934	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563416387	chr12:21018935-21018936	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528997680	chr12:21018939-21018940	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs117239853	chr12:21018956-21018957	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75393367	chr12:21018967-21018968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21364760	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:202 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21006600-21018000	Weak transcription	A549	lung
2	chr12:21015400-21018400	Strong transcription	Liver	Liver
3	chr12:21017800-21019200	Enhancers	HUVEC	blood vessel
4	chr12:21018000-21018200	Strong transcription	A549	lung
5	chr12:21018200-21018800	Weak transcription	A549	lung
6	chr12:21018400-21020800	Weak transcription	Liver	Liver
7	chr12:21018800-21020600	Strong transcription	A549	lung
8	chr12:21019800-21020000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:21020000-21020400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:21020000-21020600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:21020600-21021600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:21020600-21027400	Weak transcription	A549	lung
13	chr12:21020800-21021200	Strong transcription	Liver	Liver
14	chr12:21020800-21021600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:21021200-21024600	Weak transcription	Liver	Liver
16	chr12:21021600-21022200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:21024600-21026200	Strong transcription	Liver	Liver
18	chr12:21026200-21027800	Weak transcription	Liver	Liver
19	chr12:21027400-21028400	Strong transcription	A549	lung
20	chr12:21027800-21029600	Strong transcription	Liver	Liver
21	chr12:21028400-21035800	Weak transcription	A549	lung
22	chr12:21029600-21032400	Weak transcription	Liver	Liver
23	chr12:21032400-21035400	Strong transcription	Liver	Liver
24	chr12:21034000-21034200	Enhancers	Rectal Smooth Muscle	rectum
25	chr12:21034400-21035000	Enhancers	Stomach Mucosa	stomach
26	chr12:21034400-21035600	Weak transcription	Rectal Smooth Muscle	rectum
27	chr12:21035000-21035400	Weak transcription	Stomach Mucosa	stomach
28	chr12:21035400-21036000	Enhancers	Stomach Mucosa	stomach
29	chr12:21035400-21039000	Weak transcription	Liver	Liver
30	chr12:21035600-21036200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:21035600-21036600	Enhancers	Rectal Smooth Muscle	rectum
32	chr12:21035600-21037800	Enhancers	Colon Smooth Muscle	Colon
33	chr12:21035800-21036600	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr12:21035800-21037000	Enhancers	Adipose Nuclei	Adipose
35	chr12:21035800-21037600	Enhancers	HUVEC	blood vessel
36	chr12:21035800-21038200	Enhancers	A549	lung
37	chr12:21038200-21038400	Flanking Active TSS	A549	lung
38	chr12:21038400-21038800	Enhancers	A549	lung
39	chr12:21038800-21040600	Weak transcription	A549	lung
40	chr12:21039000-21040000	Strong transcription	Liver	Liver
41	chr12:21040000-21046600	Weak transcription	Liver	Liver
42	chr12:21044600-21054200	Weak transcription	A549	lung
43	chr12:21046600-21048400	Strong transcription	Liver	Liver
44	chr12:21048400-21052400	Weak transcription	Liver	Liver
45	chr12:21049800-21050200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr12:21051800-21052200	Weak transcription	Aorta	Aorta
47	chr12:21052400-21052600	Enhancers	Aorta	Aorta
48	chr12:21052400-21056000	Strong transcription	Liver	Liver
49	chr12:21054200-21056600	Strong transcription	A549	lung
50	chr12:21056000-21058200	ZNF genes & repeats	Liver	Liver

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