Variant report

Variant	nsv557796
Chromosome Location	chr12:25266203-25306458
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	chr12:25272177-25272180	K562	blood:	n/a	n/a
2	ARID3A	chr12:25283651-25283967	HepG2	liver:	n/a	n/a
3	ATF1	chr12:25304482-25304710	K562	blood:	n/a	n/a
4	CEBPB	chr12:25283568-25283967	IMR90	lung:	n/a	chr12:25283746-25283763
5	CEBPB	chr12:25283515-25284098	A549	lung:	n/a	chr12:25283746-25283763
6	CEBPB	chr12:25283582-25283939	H1-hESC	embryonic stem cell:	n/a	chr12:25283746-25283763
7	CEBPB	chr12:25283648-25283980	HepG2	liver:	n/a	chr12:25283746-25283763
8	CEBPB	chr12:25283539-25283909	ECC-1	luminal epithelium:	n/a	chr12:25283746-25283763
9	CEBPB	chr12:25283592-25283972	Hela-S3	cervix:	n/a	chr12:25283746-25283763
10	CEBPB	chr12:25284212-25284668	HepG2	liver:	n/a	chr12:25284651-25284662 chr12:25284651-25284662
11	CEBPB	chr12:25304380-25304975	IMR90	lung:	n/a	n/a
12	CEBPB	chr12:25283598-25283937	K562	blood:	n/a	chr12:25283746-25283763
13	CEBPB	chr12:25284243-25284585	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:25283521-25284033	HCT-116	colon:	n/a	chr12:25283746-25283763
15	CEBPB	chr12:25295575-25295638	A549	lung:	n/a	chr12:25295577-25295588
16	CEBPB	chr12:25283568-25283950	K562	blood:	n/a	chr12:25283746-25283763
17	CEBPB	chr12:25283601-25283928	A549	lung:	n/a	chr12:25283746-25283763
18	CEBPB	chr12:25283533-25283988	MCF-7	breast:	n/a	chr12:25283746-25283763
19	CHD1	chr12:25272236-25272257	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr12:25288848-25289090	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr12:25272034-25272262	GM12878	blood:	n/a	n/a
22	CTCF	chr12:25304360-25304510	AG04449	skin:	n/a	n/a
23	CTCF	chr12:25288768-25289206	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr12:25288940-25289090	NB4	blood:	n/a	n/a
25	CTCF	chr12:25272160-25272310	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:25283780-25283930	HBMEC	blood vessel:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
27	CTCF	chr12:25272160-25272310	HCM	heart:	n/a	n/a
28	CTCF	chr12:25272020-25272170	GM12871	blood:	n/a	n/a
29	CTCF	chr12:25283800-25283950	SK-N-SH_RA	brain:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
30	CTCF	chr12:25288880-25289030	NHEK	skin:	n/a	n/a
31	CTCF	chr12:25271236-25271320	NHEK	skin:	n/a	n/a
32	CTCF	chr12:25288680-25288830	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr12:25272096-25272226	GM10266	blood:	n/a	n/a
34	CTCF	chr12:25283745-25283906	Hela-S3	cervix:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
35	CTCF	chr12:25271964-25272334	GM12878	blood:	n/a	n/a
36	CTCF	chr12:25283780-25283930	MCF-7	breast:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
37	CTCF	chr12:25272040-25272190	BE2_C	brain:	n/a	n/a
38	CTCF	chr12:25288917-25289073	NHEK	skin:	n/a	n/a
39	CTCF	chr12:25283771-25283874	GM13976	blood:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
40	CTCF	chr12:25283780-25283930	HPAF	blood vessel:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
41	CTCF	chr12:25288920-25289070	GM12864	blood:	n/a	n/a
42	CTCF	chr12:25283757-25283928	GM10248	blood:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
43	CTCF	chr12:25283720-25283870	AG10803	skin:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
44	CTCF	chr12:25272120-25272270	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr12:25271226-25271278	GM19239	blood:	n/a	n/a
46	CTCF	chr12:25283720-25283870	GM12873	blood:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
47	CTCF	chr12:25272060-25272210	GM12878	blood:	n/a	n/a
48	CTCF	chr12:25283702-25283956	Pancreas_OC	pancreas:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
49	CTCF	chr12:25283700-25283850	SAEC	small airway:	n/a	chr12:25283811-25283827 chr12:25283815-25283823 chr12:25283805-25283826 chr12:25283810-25283828
50	CTCF	chr12:25272080-25272230	GM12866	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:25304568-25304618	HNPCEpiC	eye:	n/a
2	chr12:25304568-25304618	ovcar-3	ovarian:	n/a
3	chr12:25304568-25304618	SK-N-SH_RA	brain:	n/a
4	chr12:25304568-25304618	NB4	blood:	n/a
5	chr12:25304568-25304618	Caco-2	colon:	n/a
6	chr12:25304568-25304618	T-47D	breast:	n/a
7	chr12:25304568-25304618	SKMC	muscle:	n/a
8	chr12:25304568-25304618	Hela-S3	cervix:	n/a
9	chr12:25304568-25304618	BJ	skin:	n/a
10	chr12:25304568-25304618	PANC-1	pancreas:	n/a
11	chr12:25304568-25304618	HIPEpiC	eye:	n/a
12	chr12:25304568-25304618	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:25304568-25304618	AG09319	gingival:	n/a
14	chr12:25304568-25304618	SK-N-SH	brain:	n/a
15	chr12:25304568-25304618	AG09309	skin:	n/a
16	chr12:25304568-25304618	K562	blood:	n/a
17	chr12:25304568-25304618	GM12878	blood:	n/a
18	chr12:25304568-25304618	HUVEC	blood vessel:	n/a
19	chr12:25304568-25304618	AG04449	skin:	fetal
20	chr12:25304568-25304618	AG10803	skin:	n/a
21	chr12:25304568-25304618	HRE	kidney:	n/a
22	chr12:25304568-25304618	HCF	heart:	n/a
23	chr12:25304568-25304618	HEK293	kidney:	embryo
24	chr12:25304568-25304618	PrEC	prostate:	n/a
25	chr12:25304568-25304618	HCM	heart:	n/a
26	chr12:25304568-25304618	A549	lung:	n/a
27	chr12:25304568-25304618	LNCaP	prostate:	n/a
28	chr12:25304568-25304618	ProgFib	skin:	n/a
29	chr12:25304568-25304618	MCF-7	breast:	n/a
30	chr12:25304568-25304618	SK-N-MC	brain:	n/a
31	chr12:25304568-25304618	SAEC	small airway:	n/a
32	chr12:25304568-25304618	CMK	blood:	n/a
33	chr12:25304568-25304618	HRPEpiC	eye:	n/a
34	chr12:25304568-25304618	U87	brain:	n/a
35	chr12:25304568-25304618	Hepatocyte	liver:	n/a
36	chr12:25304568-25304618	AG04450	lung:	fetal
37	chr12:25304568-25304618	GM19239	blood:	n/a
38	chr12:25304568-25304618	HRCEpiC	kidney:	n/a
39	chr12:25304568-25304618	ECC-1	luminal epithelium:	n/a
40	chr12:25304568-25304618	NT2-D1	testis:	n/a
41	chr12:25304568-25304618	HepG2	liver:	n/a
42	chr12:25304568-25304618	GM12891	blood:	n/a
43	chr12:25304568-25304618	HL-60	blood:	n/a
44	chr12:25304568-25304618	NHBE	bronchial:	n/a
45	chr12:25304568-25304618	HAEpiC	amniotic membrane:	n/a
46	chr12:25304568-25304618	PFSK-1	brain:	n/a
47	chr12:25304568-25304618	GM12892	blood:	n/a
48	chr12:25304568-25304618	HMEC	breast:	n/a
49	chr12:25304568-25304618	NH-A	brain:	n/a
50	chr12:25304568-25304618	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr12:25144178..25145423-chr12:25271630..25272711,4	MCF-7	breast:
2	chr12:25005092..25005668-chr12:25271970..25272610,3	MCF-7	breast:
3	chr12:25273688..25275976-chr12:25280095..25282092,2	K562	blood:
4	chr12:25143896..25146815-chr12:25280565..25283315,2	MCF-7	breast:
5	chr12:25273688..25275976-chr12:25280095..25282092,2	K562	blood:
6	chr12:25293184..25295651-chr12:25296801..25299581,2	K562	blood:
7	chr12:25102694..25105038-chr12:25299270..25301351,2	MCF-7	breast:
8	chr12:25283942..25285554-chr12:25289504..25292032,2	K562	blood:
9	chr12:25144337..25145003-chr12:25283318..25284116,2	K562	blood:
10	chr12:25293184..25295651-chr12:25296801..25299581,2	K562	blood:
11	chr12:25112900..25113752-chr12:25283318..25284098,2	K562	blood:
12	chr12:25283942..25285554-chr12:25289504..25292032,2	K562	blood:
13	chr12:25144639..25145222-chr12:25283398..25284249,2	MCF-7	breast:
14	chr12:25284083..25286578-chr6:21600707..21602481,2	MCF-7	breast:
15	chr12:25297460..25298286-chr6:10162370..10163071,2	MCF-7	breast:
16	chr12:25282337..25284646-chr12:25539223..25540773,2	K562	blood:

Variant related genes	Relation type
CASC1	TF binding region
CASC1	CpG island
ENSG00000220771	chromatin interactions

Extended variants
information (count: 1500 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1500 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10842470	chr12:25266203-25266204	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200019747	chr12:25266214-25266215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200951965	chr12:25266250-25266251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550363008	chr12:25266275-25266276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534129970	chr12:25266303-25266304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565582005	chr12:25266321-25266322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532651577	chr12:25266323-25266324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551405481	chr12:25266339-25266340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1693360	chr12:25266353-25266354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs533925212	chr12:25266387-25266388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548644692	chr12:25266388-25266389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs187699865	chr12:25266390-25266391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537664251	chr12:25266418-25266419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182777615	chr12:25266422-25266423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553666774	chr12:25266433-25266434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149734680	chr12:25266436-25266437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539113321	chr12:25266438-25266439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555852309	chr12:25266443-25266444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577871380	chr12:25266487-25266488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538552535	chr12:25266514-25266515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs554178395	chr12:25266523-25266524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191384917	chr12:25266553-25266554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369028359	chr12:25266604-25266605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs543015254	chr12:25266628-25266629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575582879	chr12:25266719-25266720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11047843	chr12:25266794-25266795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs11047844	chr12:25266796-25266797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576565940	chr12:25266812-25266813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112532652	chr12:25266873-25266874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7954091	chr12:25266880-25266881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143738706	chr12:25266882-25266883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372667840	chr12:25266883-25266884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141465478	chr12:25266885-25266886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7954093	chr12:25266886-25266887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544036059	chr12:25266890-25266891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565336987	chr12:25266926-25266927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532884454	chr12:25266948-25266949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11047845	chr12:25266983-25266984	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs560120196	chr12:25267037-25267038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575014364	chr12:25267051-25267052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144361824	chr12:25267104-25267105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377443373	chr12:25267105-25267106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145430376	chr12:25267108-25267109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183520749	chr12:25267119-25267120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548533991	chr12:25267120-25267121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141187087	chr12:25267143-25267144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187061445	chr12:25267155-25267156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549610133	chr12:25267165-25267166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571344521	chr12:25267167-25267168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370301826	chr12:25267203-25267204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
Basal cell lymphoma	17053054	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
Breast cancer	17133270	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung adenocarcinoma	17982442	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Cancer	20164920	CNVD
Gastric cancer	22315472	CNVD
Adenocarcinoma	19001599	CNVD
Non-small cell lung cancer	19001599	CNVD
Pancreatic cancer	20981101	CNVD
Squamous cell cancer	19001599	CNVD
Acute lymphoblastic leukemia	21680795	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung cancer	18379350	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic cancer	21811562	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:25251800-25274600	Weak transcription	Pancreas	Pancrea
2	chr12:25261000-25268400	Weak transcription	Liver	Liver
3	chr12:25263600-25267600	Weak transcription	Thymus	Thymus
4	chr12:25263600-25268600	Weak transcription	GM12878-XiMat	blood
5	chr12:25263800-25267400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr12:25263800-25288800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr12:25265000-25266600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr12:25268000-25268400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:25268000-25268400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr12:25268000-25268400	Enhancers	Osteobl	bone
11	chr12:25268400-25268600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:25268400-25268600	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr12:25268400-25269000	Enhancers	HepG2	liver
14	chr12:25268400-25269200	Enhancers	Liver	Liver
15	chr12:25268600-25269000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:25268600-25269000	Enhancers	Fetal Kidney	kidney
17	chr12:25268600-25269000	Enhancers	GM12878-XiMat	blood
18	chr12:25268600-25269000	Enhancers	NHEK	skin
19	chr12:25268600-25279400	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr12:25274200-25275000	Enhancers	Osteobl	bone
21	chr12:25274400-25275200	Enhancers	Muscle Satellite Cultured Cells	--
22	chr12:25274400-25277600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:25274600-25275000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:25274600-25275400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr12:25275000-25275200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:25275200-25276200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:25275200-25277800	Enhancers	HMEC	breast
28	chr12:25276200-25277800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr12:25276800-25277600	Enhancers	NHEK	skin
30	chr12:25277400-25277800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:25281800-25282400	Enhancers	Primary B cells from cord blood	blood
32	chr12:25281800-25282400	Enhancers	Primary B cells from peripheral blood	blood
33	chr12:25282000-25282400	Enhancers	GM12878-XiMat	blood
34	chr12:25284400-25284600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr12:25286400-25286600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr12:25286800-25288000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr12:25286800-25304200	Weak transcription	Ovary	ovary
38	chr12:25288000-25289400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr12:25288000-25289400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr12:25288000-25289400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:25288000-25289600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr12:25288000-25289600	Enhancers	HMEC	breast
43	chr12:25288200-25288600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr12:25288200-25289200	Enhancers	Esophagus	oesophagus
45	chr12:25288200-25289400	Enhancers	NHEK	skin
46	chr12:25288200-25289600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:25288400-25288800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr12:25288400-25289000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr12:25288400-25289000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:25288400-25289200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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