Variant report

Variant	nsv1035141
Chromosome Location	chr12:20286595-20429040
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	ARID3A	chr12:20328706-20329235	HepG2	liver:	n/a	n/a
2	ATF2	chr12:20297246-20297708	GM12878	blood:	n/a	n/a
3	ATF2	chr12:20417402-20417869	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr12:20417391-20417877	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr12:20365619-20366130	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:20297229-20297703	GM12878	blood:	n/a	n/a
7	ATF2	chr12:20365538-20366144	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr12:20365498-20366048	A549	lung:	n/a	chr12:20365714-20365725
9	ATF3	chr12:20365508-20366043	A549	lung:	n/a	chr12:20365714-20365725
10	BACH1	chr12:20365601-20366054	H1-hESC	embryonic stem cell:	n/a	chr12:20365815-20365829
11	BATF	chr12:20340989-20341339	GM12878	blood:	n/a	chr12:20341161-20341172
12	BATF	chr12:20295925-20296216	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:20297361-20297613	GM12878	blood:	n/a	n/a
14	BCL3	chr12:20365443-20366394	A549	lung:	n/a	chr12:20365645-20365654
15	BCL3	chr12:20365487-20366182	A549	lung:	n/a	chr12:20365645-20365654
16	BHLHE40	chr12:20297305-20297951	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:20293717-20294055	GM12878	blood:	n/a	n/a
18	BRCA1	chr12:20365472-20366530	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr12:20365455-20366135	HCT-116	colon:	n/a	n/a
20	CBX3	chr12:20347140-20347573	HCT-116	colon:	n/a	n/a
21	CBX3	chr12:20365485-20366142	HCT-116	colon:	n/a	n/a
22	CEBPB	chr12:20366768-20367667	Hela-S3	cervix:	n/a	chr12:20366958-20366969 chr12:20366957-20366970 chr12:20366959-20366968
23	CEBPB	chr12:20407920-20408214	A549	lung:	n/a	chr12:20408021-20408032 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408021-20408034 chr12:20408071-20408084
24	CEBPB	chr12:20365414-20366173	ECC-1	luminal epithelium:	n/a	chr12:20365678-20365689
25	CEBPB	chr12:20366806-20367147	A549	lung:	n/a	chr12:20366958-20366969 chr12:20366957-20366970 chr12:20366959-20366968
26	CEBPB	chr12:20366785-20367124	IMR90	lung:	n/a	chr12:20366958-20366969 chr12:20366957-20366970 chr12:20366959-20366968
27	CEBPB	chr12:20365509-20366034	A549	lung:	n/a	chr12:20365678-20365689
28	CEBPB	chr12:20365504-20366047	A549	lung:	n/a	chr12:20365678-20365689
29	CEBPB	chr12:20417517-20417854	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:20303749-20304367	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr12:20371025-20371512	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr12:20407912-20408217	HepG2	liver:	n/a	chr12:20408021-20408032 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408021-20408034 chr12:20408071-20408084
33	CEBPB	chr12:20407936-20408212	H1-hESC	embryonic stem cell:	n/a	chr12:20408021-20408032 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408021-20408034 chr12:20408071-20408084
34	CEBPB	chr12:20366697-20367218	A549	lung:	n/a	chr12:20366958-20366969 chr12:20366957-20366970 chr12:20366959-20366968
35	CEBPB	chr12:20341277-20341393	HepG2	liver:	n/a	chr12:20341331-20341342
36	CEBPB	chr12:20365520-20365921	IMR90	lung:	n/a	chr12:20365678-20365689
37	CEBPB	chr12:20365424-20366261	A549	lung:	n/a	chr12:20365678-20365689
38	CEBPB	chr12:20366826-20367134	HepG2	liver:	n/a	chr12:20366958-20366969 chr12:20366957-20366970 chr12:20366959-20366968
39	CEBPB	chr12:20421132-20421342	A549	lung:	n/a	n/a
40	CEBPB	chr12:20366696-20367182	ECC-1	luminal epithelium:	n/a	chr12:20366958-20366969 chr12:20366957-20366970 chr12:20366959-20366968
41	CEBPB	chr12:20366779-20367144	ECC-1	luminal epithelium:	n/a	chr12:20366958-20366969 chr12:20366957-20366970 chr12:20366959-20366968
42	CEBPB	chr12:20365266-20366365	Hela-S3	cervix:	n/a	chr12:20365678-20365689
43	CEBPB	chr12:20365609-20365909	H1-hESC	embryonic stem cell:	n/a	chr12:20365678-20365689
44	CEBPB	chr12:20407928-20408192	Hela-S3	cervix:	n/a	chr12:20408021-20408032 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408021-20408034 chr12:20408071-20408084
45	CEBPB	chr12:20334187-20334599	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr12:20365447-20366139	ECC-1	luminal epithelium:	n/a	chr12:20365678-20365689
47	CEBPB	chr12:20394617-20394791	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:20407920-20408213	IMR90	lung:	n/a	chr12:20408021-20408032 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408073-20408082 chr12:20408021-20408034 chr12:20408071-20408084
49	CHD2	chr12:20365650-20366037	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr12:20365491-20366237	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:20336617-20336667	GM12878	blood:	n/a
2	chr12:20336617-20336667	PFSK-1	brain:	n/a
3	chr12:20336617-20336667	HIPEpiC	eye:	n/a
4	chr12:20365720-20365770	AG09319	gingival:	n/a
5	chr12:20365720-20365770	PrEC	prostate:	n/a
6	chr12:20336617-20336667	MCF10A-Er-Src	breast:	n/a
7	chr12:20336617-20336667	GM12892	blood:	n/a
8	chr12:20365720-20365770	PFSK-1	brain:	n/a
9	chr12:20336617-20336667	HPAEpiC	pulmonary alveolar:	n/a
10	chr12:20365720-20365770	NHBE	bronchial:	n/a
11	chr12:20365720-20365770	AG04450	lung:	fetal
12	chr12:20336617-20336667	HEK293	kidney:	embryo
13	chr12:20336617-20336667	HepG2	liver:	n/a
14	chr12:20336617-20336667	NHBE	bronchial:	n/a
15	chr12:20365720-20365770	NH-A	brain:	n/a
16	chr12:20336617-20336667	Hela-S3	cervix:	n/a
17	chr12:20336617-20336667	IMR90	lung:	fetal
18	chr12:20365720-20365770	HNPCEpiC	eye:	n/a
19	chr12:20365720-20365770	AG04449	skin:	fetal
20	chr12:20365720-20365770	BE2_C	brain:	n/a
21	chr12:20336617-20336667	NHDF-neo	bronchial:	n/a
22	chr12:20336617-20336667	HRPEpiC	eye:	n/a
23	chr12:20336617-20336667	HCT-116	colon:	n/a
24	chr12:20365720-20365770	SK-N-MC	brain:	n/a
25	chr12:20336617-20336667	H1-hESC	embryonic stem cell:	embryo
26	chr12:20336617-20336667	GM06990	blood:	n/a
27	chr12:20365720-20365770	SAEC	small airway:	n/a
28	chr12:20365720-20365770	HRCEpiC	kidney:	n/a
29	chr12:20336617-20336667	PrEC	prostate:	n/a
30	chr12:20336617-20336667	T-47D	breast:	n/a
31	chr12:20365720-20365770	A549	lung:	n/a
32	chr12:20365720-20365770	GM12892	blood:	n/a
33	chr12:20336617-20336667	AG04449	skin:	fetal
34	chr12:20336617-20336667	AG04450	lung:	fetal
35	chr12:20336617-20336667	AoSMC	blood vessel:	n/a
36	chr12:20365720-20365770	PANC-1	pancreas:	n/a
37	chr12:20336617-20336667	SK-N-MC	brain:	n/a
38	chr12:20365720-20365770	MCF-7	breast:	n/a
39	chr12:20365720-20365770	HRE	kidney:	n/a
40	chr12:20336617-20336667	LNCaP	prostate:	n/a
41	chr12:20336617-20336667	AG09309	skin:	n/a
42	chr12:20365720-20365770	Caco-2	colon:	n/a
43	chr12:20365720-20365770	HUVEC	blood vessel:	n/a
44	chr12:20336617-20336667	HCF	heart:	n/a
45	chr12:20365720-20365770	GM12891	blood:	n/a
46	chr12:20336617-20336667	Hepatocyte	liver:	n/a
47	chr12:20336617-20336667	ECC-1	luminal epithelium:	n/a
48	chr12:20365720-20365770	HMEC	breast:	n/a
49	chr12:20365720-20365770	HAEpiC	amniotic membrane:	n/a
50	chr12:20336617-20336667	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:20299715..20301403-chr21:38005000..38006593,2	MCF-7	breast:
2	chr12:20068451..20069047-chr12:20373146..20373740,2	MCF-7	breast:
3	chr12:20357513..20360077-chr12:20436701..20439478,2	K562	blood:
4	chr12:20357490..20359310-chr12:20364032..20366032,2	MCF-7	breast:
5	chr12:20291329..20292956-chr12:20366236..20367919,2	K562	blood:
6	chr12:20305592..20306482-chr5:102206551..102207078,2	MCF-7	breast:
7	chr12:20357490..20359310-chr12:20364032..20366032,2	MCF-7	breast:
8	chr12:19891960..19892749-chr12:20373098..20373845,3	MCF-7	breast:
9	chr12:20291329..20292956-chr12:20366236..20367919,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO1A2-2	chr12:20399536-20399565	XLOC_010028
2	lnc-SLCO1A2-2	chr12:20387841-20388052	XLOC_010028
3	lnc-SLCO1A2-2	chr12:20417034-20417097	XLOC_010028

Variant related genes	Relation type
ENSG00000256499	TF binding region
ENSG00000256499	CpG island

Extended variants
information (count: 4266 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:4266 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575557956	chr12:20286635-20286636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112231261	chr12:20286657-20286658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544447621	chr12:20286697-20286698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577596091	chr12:20286706-20286707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113653451	chr12:20286770-20286771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188303680	chr12:20286786-20286787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs141224357	chr12:20286810-20286811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199524218	chr12:20286815-20286816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530312609	chr12:20286816-20286817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192940625	chr12:20286834-20286835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79463885	chr12:20286870-20286871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78923830	chr12:20286874-20286875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560036304	chr12:20286960-20286961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376045623	chr12:20286989-20286990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4762931	chr12:20287009-20287010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565549365	chr12:20287012-20287013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531081939	chr12:20287048-20287049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75610493	chr12:20287062-20287063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567281543	chr12:20287064-20287065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536346804	chr12:20287085-20287086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs11045063	chr12:20287145-20287146	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs11045064	chr12:20287148-20287149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs11045065	chr12:20287159-20287160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149852344	chr12:20287248-20287249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144250155	chr12:20287267-20287268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557641717	chr12:20287270-20287271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139483405	chr12:20287272-20287273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560179331	chr12:20287300-20287301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148713857	chr12:20287318-20287319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11045066	chr12:20287404-20287405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35280204	chr12:20287429-20287430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs142737755	chr12:20287450-20287451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35149001	chr12:20287453-20287454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573676754	chr12:20287480-20287481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542786164	chr12:20287532-20287533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570279146	chr12:20287542-20287543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150587349	chr12:20287545-20287546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369050732	chr12:20287548-20287549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140558538	chr12:20287553-20287554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12320405	chr12:20287562-20287563	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs182847644	chr12:20287586-20287587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569145439	chr12:20287608-20287609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373730380	chr12:20287628-20287629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187875269	chr12:20287711-20287712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191258778	chr12:20287743-20287744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560991166	chr12:20287762-20287763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567871536	chr12:20287830-20287831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10841450	chr12:20287852-20287853	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs546721505	chr12:20287856-20287857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114145500	chr12:20287907-20287908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20258800-20327400	Weak transcription	Aorta	Aorta
2	chr12:20268600-20289200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:20279800-20289000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr12:20280600-20295000	Weak transcription	Colon Smooth Muscle	Colon
5	chr12:20286000-20288800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:20288200-20288600	Enhancers	Fetal Muscle Trunk	muscle
7	chr12:20288800-20289800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:20289200-20289800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:20289400-20289800	Enhancers	Fetal Heart	heart
10	chr12:20293800-20294400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr12:20295000-20295600	Enhancers	Fetal Stomach	stomach
12	chr12:20295000-20296000	Enhancers	Colon Smooth Muscle	Colon
13	chr12:20295000-20296200	Enhancers	Rectal Smooth Muscle	rectum
14	chr12:20295200-20296000	Enhancers	Fetal Lung	lung
15	chr12:20295200-20296200	Enhancers	Stomach Smooth Muscle	stomach
16	chr12:20295200-20296400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr12:20296600-20297400	Enhancers	GM12878-XiMat	blood
18	chr12:20303400-20304400	Enhancers	HUVEC	blood vessel
19	chr12:20303600-20304000	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr12:20303600-20304200	Enhancers	Fetal Intestine Small	intestine
21	chr12:20303600-20304400	Enhancers	Fetal Kidney	kidney
22	chr12:20303800-20304200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:20303800-20304400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr12:20303800-20304400	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr12:20304000-20304400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr12:20304200-20307200	Weak transcription	Fetal Intestine Small	intestine
27	chr12:20306800-20308800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:20306800-20308800	Enhancers	Dnd41	blood
29	chr12:20306800-20309000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:20307000-20307400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:20307000-20307400	Enhancers	Adipose Nuclei	Adipose
32	chr12:20307000-20307400	Enhancers	Colon Smooth Muscle	Colon
33	chr12:20307000-20308200	Enhancers	Hela-S3	cervix
34	chr12:20307200-20307400	Flanking Active TSS	Liver	Liver
35	chr12:20307200-20307400	Enhancers	GM12878-XiMat	blood
36	chr12:20307200-20307600	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr12:20307200-20307600	Enhancers	Fetal Intestine Small	intestine
38	chr12:20307200-20307600	Enhancers	NHDF-Ad	bronchial
39	chr12:20307200-20307600	Active TSS	Osteobl	bone
40	chr12:20307200-20308800	Enhancers	Primary hematopoietic stem cells	blood
41	chr12:20307200-20309000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr12:20307400-20307600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:20307400-20307600	Active TSS	Liver	Liver
44	chr12:20307800-20308600	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr12:20307800-20308800	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr12:20313800-20314200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr12:20322200-20322600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:20327400-20327800	Enhancers	Fetal Intestine Small	intestine
49	chr12:20327400-20327800	Enhancers	Lung	lung
50	chr12:20327400-20328200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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