Variant report

Variant	esv3402095
Chromosome Location	chr12:46937340-46983181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1100)
CpG islands
(count:244)
Chromatin interactive
region (count:52)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:46949884-46950318	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:46950838-46951415	K562	blood:	n/a	n/a
3	ARID3A	chr12:46940745-46940955	K562	blood:	n/a	n/a
4	ARID3A	chr12:46970849-46971198	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:46951808-46952106	K562	blood:	n/a	n/a
6	ARID3A	chr12:46947193-46947453	K562	blood:	n/a	n/a
7	ARID3A	chr12:46943543-46943961	K562	blood:	n/a	n/a
8	ARID3A	chr12:46949955-46949974	K562	blood:	n/a	n/a
9	ARID3A	chr12:46973105-46973651	HepG2	liver:	n/a	n/a
10	ATF1	chr12:46963685-46963955	K562	blood:	n/a	n/a
11	ATF1	chr12:46950774-46951297	K562	blood:	n/a	n/a
12	ATF1	chr12:46979675-46979881	K562	blood:	n/a	n/a
13	ATF1	chr12:46947030-46947442	K562	blood:	n/a	n/a
14	ATF1	chr12:46951686-46952097	K562	blood:	n/a	n/a
15	ATF1	chr12:46943561-46943940	K562	blood:	n/a	n/a
16	ATF1	chr12:46940765-46941036	K562	blood:	n/a	n/a
17	ATF1	chr12:46956215-46956302	K562	blood:	n/a	n/a
18	ATF2	chr12:46940596-46941047	GM12878	blood:	n/a	n/a
19	ATF3	chr12:46943355-46944097	HCT-116	colon:	n/a	n/a
20	ATF3	chr12:46943504-46944025	K562	blood:	n/a	n/a
21	ATF3	chr12:46946969-46947564	HCT-116	colon:	n/a	n/a
22	ATF3	chr12:46951623-46952152	HCT-116	colon:	n/a	n/a
23	ATF3	chr12:46951638-46952138	K562	blood:	n/a	n/a
24	BATF	chr12:46949177-46949431	GM12878	blood:	n/a	chr12:46949323-46949334
25	BHLHE40	chr12:46963606-46963877	K562	blood:	n/a	n/a
26	BHLHE40	chr12:46940758-46941097	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:46943444-46944055	K562	blood:	n/a	n/a
28	BHLHE40	chr12:46940808-46941033	K562	blood:	n/a	n/a
29	BHLHE40	chr12:46950000-46950071	K562	blood:	n/a	n/a
30	BRCA1	chr12:46943497-46944043	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr12:46956223-46957069	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr12:46949297-46950423	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr12:46946949-46947554	HCT-116	colon:	n/a	n/a
34	CBX3	chr12:46961583-46961774	K562	blood:	n/a	n/a
35	CBX3	chr12:46943252-46944057	HCT-116	colon:	n/a	n/a
36	CBX3	chr12:46950483-46951126	HCT-116	colon:	n/a	n/a
37	CBX3	chr12:46943508-46944158	K562	blood:	n/a	n/a
38	CBX3	chr12:46979624-46980018	K562	blood:	n/a	n/a
39	CBX3	chr12:46949671-46950430	HCT-116	colon:	n/a	n/a
40	CBX3	chr12:46946883-46947968	HCT-116	colon:	n/a	n/a
41	CCNT2	chr12:46943377-46943774	K562	blood:	n/a	n/a
42	CCNT2	chr12:46950979-46951229	K562	blood:	n/a	n/a
43	CCNT2	chr12:46940629-46940879	K562	blood:	n/a	n/a
44	CEBPB	chr12:46973446-46973680	MCF-7	breast:	n/a	n/a
45	CEBPB	chr12:46947070-46947526	A549	lung:	n/a	n/a
46	CEBPB	chr12:46943151-46944313	HCT-116	colon:	n/a	chr12:46943789-46943800 chr12:46944096-46944109 chr12:46944096-46944107 chr12:46944096-46944107
47	CEBPB	chr12:46943361-46944218	IMR90	lung:	n/a	chr12:46943789-46943800 chr12:46944096-46944109 chr12:46944096-46944107 chr12:46944096-46944107
48	CEBPB	chr12:46974243-46974591	Hela-S3	cervix:	n/a	chr12:46974404-46974415
49	CEBPB	chr12:46943591-46944099	K562	blood:	n/a	chr12:46943789-46943800
50	CEBPB	chr12:46974302-46974450	HepG2	liver:	n/a	chr12:46974404-46974415

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:46950853-46950903	BE2_C	brain:	n/a
2	chr12:46945908-46945958	SK-N-MC	brain:	n/a
3	chr12:46945908-46945958	HRCEpiC	kidney:	n/a
4	chr12:46948457-46948507	HCM	heart:	n/a
5	chr12:46945908-46945958	SK-N-SH_RA	brain:	n/a
6	chr12:46950853-46950903	AG09319	gingival:	n/a
7	chr12:46950853-46950903	LNCaP	prostate:	n/a
8	chr12:46945908-46945958	HUVEC	blood vessel:	n/a
9	chr12:46948457-46948507	K562	blood:	n/a
10	chr12:46941377-46941427	IMR90	lung:	fetal
11	chr12:46948457-46948507	HNPCEpiC	eye:	n/a
12	chr12:46948457-46948507	HMEC	breast:	n/a
13	chr12:46950853-46950903	GM12878	blood:	n/a
14	chr12:46950853-46950903	HEK293	kidney:	embryo
15	chr12:46950853-46950903	NHBE	bronchial:	n/a
16	chr12:46948457-46948507	HEK293	kidney:	embryo
17	chr12:46945908-46945958	AoSMC	blood vessel:	n/a
18	chr12:46945908-46945958	GM12891	blood:	n/a
19	chr12:46948457-46948507	SK-N-MC	brain:	n/a
20	chr12:46950853-46950903	Jurkat	blood:	n/a
21	chr12:46941377-46941427	U87	brain:	n/a
22	chr12:46941377-46941427	CMK	blood:	n/a
23	chr12:46950853-46950903	AoSMC	blood vessel:	n/a
24	chr12:46941377-46941427	PrEC	prostate:	n/a
25	chr12:46948457-46948507	SAEC	small airway:	n/a
26	chr12:46950853-46950903	T-47D	breast:	n/a
27	chr12:46948457-46948507	T-47D	breast:	n/a
28	chr12:46950853-46950903	HAEpiC	amniotic membrane:	n/a
29	chr12:46941377-46941427	HCM	heart:	n/a
30	chr12:46950853-46950903	HPAEpiC	pulmonary alveolar:	n/a
31	chr12:46948457-46948507	Jurkat	blood:	n/a
32	chr12:46950853-46950903	NHDF-neo	bronchial:	n/a
33	chr12:46948457-46948507	AG09309	skin:	n/a
34	chr12:46941377-46941427	HL-60	blood:	n/a
35	chr12:46945908-46945958	GM12878	blood:	n/a
36	chr12:46950853-46950903	RPTEC	kidney:	n/a
37	chr12:46941377-46941427	GM06990	blood:	n/a
38	chr12:46941377-46941427	GM19239	blood:	n/a
39	chr12:46950853-46950903	HUVEC	blood vessel:	n/a
40	chr12:46945908-46945958	AG09319	gingival:	n/a
41	chr12:46948457-46948507	HepG2	liver:	n/a
42	chr12:46948457-46948507	NT2-D1	testis:	n/a
43	chr12:46948457-46948507	CMK	blood:	n/a
44	chr12:46948457-46948507	AG04450	lung:	fetal
45	chr12:46950853-46950903	SK-N-MC	brain:	n/a
46	chr12:46945908-46945958	K562	blood:	n/a
47	chr12:46948457-46948507	LNCaP	prostate:	n/a
48	chr12:46941377-46941427	AG09319	gingival:	n/a
49	chr12:46948457-46948507	HRPEpiC	eye:	n/a
50	chr12:46945908-46945958	NH-A	brain:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:46769477..46772174-chr12:46953105..46955870,2	K562	blood:
2	chr12:46775028..46778890-chr12:46944542..46947294,5	K562	blood:
3	chr12:46886568..46889250-chr12:46940545..46943079,3	MCF-7	breast:
4	chr12:46965755..46967970-chr12:46969956..46972326,2	MCF-7	breast:
5	chr12:46760939..46762662-chr12:46964793..46967282,2	K562	blood:
6	chr12:46764440..46766646-chr12:46971360..46973081,2	MCF-7	breast:
7	chr12:46947119..46948871-chr12:46950791..46952995,2	K562	blood:
8	chr12:46750303..46751905-chr12:46962161..46964457,2	K562	blood:
9	chr12:46944404..46946357-chr12:46950000..46951515,2	K562	blood:
10	chr12:46777594..46781632-chr12:46950708..46954410,5	K562	blood:
11	chr12:46963166..46965349-chr12:46968243..46970653,2	K562	blood:
12	chr12:46766323..46768066-chr12:46942252..46945383,3	K562	blood:
13	chr12:46944404..46946357-chr12:46950000..46951515,2	K562	blood:
14	chr12:46758492..46761317-chr12:46945158..46946855,2	K562	blood:
15	chr12:46765738..46767413-chr12:46961287..46963131,2	MCF-7	breast:
16	chr12:46952895..46955574-chr12:46956120..46958944,2	K562	blood:
17	chr12:46750618..46753866-chr12:46950440..46953586,3	K562	blood:
18	chr12:46943748..46944525-chr19:45970915..45971467,2	Hela-S3	cervix:
19	chr12:46887354..46888000-chr12:46973431..46973941,2	MCF-7	breast:
20	chr12:46776357..46779277-chr12:46958774..46961528,2	K562	blood:
21	chr12:46940433..46942462-chr12:46951225..46953881,2	MCF-7	breast:
22	chr12:46763720..46767823-chr12:46939612..46944083,5	K562	blood:
23	chr12:46661324..46663947-chr12:46944457..46946372,2	MCF-7	breast:
24	chr12:46775028..46778890-chr12:46944672..46947294,3	K562	blood:
25	chr12:46778324..46780021-chr12:46941195..46943535,2	K562	blood:
26	chr12:46942932..46945589-chr12:46948248..46950851,2	MCF-7	breast:
27	chr12:46963166..46965349-chr12:46968243..46970653,2	K562	blood:
28	chr12:46941171..46945201-chr12:46945236..46949422,7	K562	blood:
29	chr12:46765212..46766815-chr12:46968840..46971660,2	MCF-7	breast:
30	chr12:46765109..46767382-chr12:46939505..46942259,2	MCF-7	breast:
31	chr12:46748960..46751313-chr12:46947807..46949856,2	MCF-7	breast:
32	chr12:46775915..46780698-chr12:46939854..46943632,6	K562	blood:
33	chr12:46921090..46923425-chr12:46940869..46943856,2	K562	blood:
34	chr12:46761162..46768544-chr12:46964631..46969835,8	K562	blood:
35	chr12:46949570..46952238-chr12:47068920..47070785,2	K562	blood:
36	chr12:46965755..46967970-chr12:46969956..46972326,2	MCF-7	breast:
37	chr12:46963166..46965705-chr12:46969153..46971844,2	K562	blood:
38	chr12:46661429..46663096-chr12:46943395..46946017,2	K562	blood:
39	chr12:46952895..46955574-chr12:46956120..46958944,2	K562	blood:
40	chr12:46942932..46945589-chr12:46948248..46950851,2	MCF-7	breast:
41	chr12:46839274..46841469-chr12:46940549..46942826,2	K562	blood:
42	chr12:46777128..46779094-chr12:46952910..46956559,3	K562	blood:
43	chr12:46940433..46942462-chr12:46951225..46953881,2	MCF-7	breast:
44	chr12:46929095..46933419-chr12:46940560..46942504,4	K562	blood:
45	chr12:46963166..46965705-chr12:46969153..46971844,2	K562	blood:
46	chr12:46764628..46766853-chr12:46959111..46963000,4	K562	blood:
47	chr12:46765496..46768188-chr12:46945105..46947805,2	K562	blood:
48	chr12:46947119..46948871-chr12:46950791..46952995,2	K562	blood:
49	chr12:46765672..46767506-chr12:46948765..46951182,2	MCF-7	breast:
50	chr12:46972689..46974788-chr12:47053934..47056734,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC38A2-3	chr12:46955020-46955380	NONHSAT027883
2	lnc-SLC38A2-3	chr12:46950130-46950267	NONHSAT027883
3	lnc-ARID2-3	chr12:46965039-46965195	ENSG00000272369.1
4	lnc-SLC38A2-3	chr12:46968827-46968899	NONHSAT027883
5	lnc-ARID2-3	chr12:46965039-46965148	XLOC_009723
6	lnc-ARID2-3	chr12:46965039-46965065	NONHSAT027872
7	lnc-SLC38A2-3	chr12:46953646-46953745	NONHSAT027883

No data

Variant related genes	Relation type
OR7A19P	TF binding region
OR7A19P	CpG island
ENSG00000134294	chromatin interactions
ENSG00000272369	chromatin interactions
ENSG00000111371	chromatin interactions
ENSG00000257496	chromatin interactions
ENSG00000258096	chromatin interactions
ENSG00000257261	chromatin interactions
ENSG00000125740	chromatin interactions
PDK4	miRNA target sites

Extended variants
information (count: 1486 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1486 , 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	rs189895004	chr12:46937396-46937397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536430438	chr12:46937397-46937398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553670044	chr12:46937410-46937411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573575040	chr12:46937418-46937419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138124160	chr12:46937422-46937423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs181535984	chr12:46937452-46937453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577831005	chr12:46937458-46937459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543479456	chr12:46937465-46937466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150558503	chr12:46937475-46937476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139584603	chr12:46937497-46937498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs202165346	chr12:46937550-46937551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186000008	chr12:46937574-46937575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559222640	chr12:46937585-46937586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576066474	chr12:46937591-46937592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528328653	chr12:46937597-46937598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551377037	chr12:46937637-46937638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190781067	chr12:46937659-46937660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537027723	chr12:46937660-46937661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149725074	chr12:46937704-46937705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181904108	chr12:46937705-46937706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs58188619	chr12:46937706-46937707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558533939	chr12:46937728-46937729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536898786	chr12:46937787-46937788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553560981	chr12:46937790-46937791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186597144	chr12:46937811-46937812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539306818	chr12:46937849-46937850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557810209	chr12:46937915-46937916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527773778	chr12:46937954-46937955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546522059	chr12:46937959-46937960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190607242	chr12:46937969-46937970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182889750	chr12:46937980-46937981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543039228	chr12:46937998-46937999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557062220	chr12:46938000-46938001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573605982	chr12:46938002-46938003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542816048	chr12:46938032-46938033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532425639	chr12:46938036-46938037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187851799	chr12:46938042-46938043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528391612	chr12:46938056-46938057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544928857	chr12:46938084-46938085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191512860	chr12:46938092-46938093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530975471	chr12:46938105-46938106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550697796	chr12:46938174-46938175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs567752246	chr12:46938232-46938233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182648582	chr12:46938241-46938242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547234276	chr12:46938321-46938322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144715531	chr12:46938325-46938326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113804354	chr12:46938352-46938353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376458592	chr12:46938388-46938389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187334072	chr12:46938392-46938393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559475307	chr12:46938443-46938444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	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
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21542898	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:46925200-46940600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:46925400-46939000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:46925400-46940200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:46925600-46940000	Weak transcription	NHEK	skin
5	chr12:46925800-46940200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr12:46926400-46939000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:46928400-46948600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr12:46930600-46938600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr12:46930600-46940000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr12:46930800-46938600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:46930800-46940200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:46933200-46940200	Weak transcription	GM12878-XiMat	blood
13	chr12:46933400-46940400	Weak transcription	HepG2	liver
14	chr12:46933800-46939600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr12:46934000-46939000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr12:46938600-46940000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
17	chr12:46938600-46941800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr12:46939000-46939400	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
19	chr12:46939000-46939400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr12:46939000-46939400	ZNF genes & repeats	Dnd41	blood
21	chr12:46939000-46939800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr12:46939000-46940600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:46939400-46940000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr12:46939400-46940000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr12:46939400-46940000	Weak transcription	Dnd41	blood
26	chr12:46939400-46940400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr12:46939600-46940000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:46939600-46944200	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr12:46939800-46940600	Enhancers	Primary T cells from cord blood	blood
30	chr12:46940000-46940200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:46940000-46940600	Weak transcription	Primary hematopoietic stem cells	blood
32	chr12:46940000-46940600	Enhancers	NHEK	skin
33	chr12:46940000-46941000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr12:46940000-46941600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr12:46940000-46941800	Enhancers	Primary B cells from peripheral blood	blood
36	chr12:46940000-46942200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr12:46940000-46942200	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr12:46940000-46942200	Enhancers	Dnd41	blood
39	chr12:46940000-46942400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:46940000-46945600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:46940200-46940400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr12:46940200-46940400	Enhancers	GM12878-XiMat	blood
43	chr12:46940200-46940800	Enhancers	HUVEC	blood vessel
44	chr12:46940200-46941000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr12:46940200-46941000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:46940200-46941000	Enhancers	Duodenum Mucosa	Duodenum
47	chr12:46940200-46941200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr12:46940200-46941400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr12:46940200-46941400	Enhancers	Primary B cells from cord blood	blood
50	chr12:46940200-46941600	Enhancers	Primary T helper cells fromperipheralblood	blood

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