Variant report

Variant	nsv455727
Chromosome Location	chr12:120259679-120420670
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1678)
CpG islands
(count:1042)
Chromatin interactive
region (count:85)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1678 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:120375926-120376099	K562	blood:	n/a	n/a
2	ARID3A	chr12:120378632-120379155	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:120315258-120315442	K562	blood:	n/a	n/a
4	ARID3A	chr12:120339836-120340277	K562	blood:	n/a	n/a
5	ATF1	chr12:120339862-120340244	K562	blood:	n/a	n/a
6	ATF1	chr12:120332155-120332188	K562	blood:	n/a	n/a
7	ATF1	chr12:120345952-120346114	K562	blood:	n/a	n/a
8	ATF1	chr12:120315072-120315468	K562	blood:	n/a	n/a
9	ATF1	chr12:120372736-120372814	K562	blood:	n/a	n/a
10	ATF2	chr12:120267247-120267575	GM12878	blood:	n/a	n/a
11	ATF2	chr12:120339831-120340186	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr12:120378664-120379412	A549	lung:	n/a	n/a
13	ATF3	chr12:120378609-120379440	A549	lung:	n/a	n/a
14	BACH1	chr12:120393976-120394069	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr12:120267208-120267621	GM12878	blood:	n/a	n/a
16	BATF	chr12:120363172-120363430	GM12878	blood:	n/a	chr12:120363270-120363281 chr12:120363251-120363262
17	BATF	chr12:120267317-120267626	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:120267219-120267546	GM12878	blood:	n/a	n/a
19	BCL3	chr12:120378622-120379141	A549	lung:	n/a	n/a
20	BCL3	chr12:120378604-120379161	A549	lung:	n/a	n/a
21	BCL3	chr12:120339757-120340322	A549	lung:	n/a	chr12:120340045-120340058
22	BCL3	chr12:120339755-120340316	A549	lung:	n/a	chr12:120340045-120340058
23	BCL3	chr12:120339841-120340170	GM12878	blood:	n/a	chr12:120340045-120340058
24	BHLHE40	chr12:120307813-120307860	K562	blood:	n/a	n/a
25	BHLHE40	chr12:120372597-120372759	K562	blood:	n/a	n/a
26	BHLHE40	chr12:120375994-120376094	K562	blood:	n/a	n/a
27	BHLHE40	chr12:120339887-120340188	K562	blood:	n/a	n/a
28	BHLHE40	chr12:120375919-120376174	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:120315152-120315534	K562	blood:	n/a	n/a
30	BRCA1	chr12:120315136-120315142	GM12878	blood:	n/a	n/a
31	BRCA1	chr12:120339806-120340206	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr12:120315408-120315575	GM12878	blood:	n/a	n/a
33	BRCA1	chr12:120314495-120314498	GM12878	blood:	n/a	n/a
34	BRCA1	chr12:120315127-120315548	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr12:120314755-120314822	HepG2	liver:	n/a	n/a
36	CBX3	chr12:120378487-120379114	HCT-116	colon:	n/a	n/a
37	CBX3	chr12:120378624-120379099	HCT-116	colon:	n/a	n/a
38	CBX3	chr12:120315052-120315639	K562	blood:	n/a	n/a
39	CBX3	chr12:120394885-120395412	HCT-116	colon:	n/a	n/a
40	CCNT2	chr12:120314810-120315189	K562	blood:	n/a	n/a
41	CEBPB	chr12:120351004-120351192	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:120266194-120266250	HepG2	liver:	n/a	chr12:120266228-120266239 chr12:120266227-120266240 chr12:120266227-120266238 chr12:120266227-120266240 chr12:120266227-120266238 chr12:120266227-120266240
43	CEBPB	chr12:120357853-120358172	MCF-7	breast:	n/a	chr12:120358037-120358048
44	CEBPB	chr12:120321576-120321767	A549	lung:	n/a	chr12:120321682-120321693
45	CEBPB	chr12:120419270-120419479	HepG2	liver:	n/a	chr12:120419338-120419349
46	CEBPB	chr12:120378284-120378580	K562	blood:	n/a	n/a
47	CEBPB	chr12:120406043-120406269	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:120378346-120379123	A549	lung:	n/a	n/a
49	CEBPB	chr12:120371327-120371339	K562	blood:	n/a	n/a
50	CEBPB	chr12:120348928-120349328	IMR90	lung:	n/a	n/a

(count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:120315168-120315218	T-47D	breast:	n/a
2	chr12:120311375-120311425	GM12878	blood:	n/a
3	chr12:120314898-120314948	NHDF-neo	bronchial:	n/a
4	chr12:120315144-120315194	NHDF-neo	bronchial:	n/a
5	chr12:120315168-120315218	ovcar-3	ovarian:	n/a
6	chr12:120315168-120315218	T-47D	breast:	n/a
7	chr12:120311375-120311425	GM12878	blood:	n/a
8	chr12:120314898-120314948	NHDF-neo	bronchial:	n/a
9	chr12:120315144-120315194	NHDF-neo	bronchial:	n/a
10	chr12:120315168-120315218	ovcar-3	ovarian:	n/a
11	chr12:120315133-120315183	GM19239	blood:	n/a
12	chr12:120315129-120315179	AG09309	skin:	n/a
13	chr12:120317798-120317848	Hepatocyte	liver:	n/a
14	chr12:120315015-120315065	AoSMC	blood vessel:	n/a
15	chr12:120315669-120315719	CMK	blood:	n/a
16	chr12:120314679-120314729	AG10803	skin:	n/a
17	chr12:120315422-120315472	MCF10A-Er-Src	breast:	n/a
18	chr12:120315144-120315194	NT2-D1	testis:	n/a
19	chr12:120315015-120315065	GM19239	blood:	n/a
20	chr12:120307689-120307739	K562	blood:	n/a
21	chr12:120315085-120315135	NT2-D1	testis:	n/a
22	chr12:120315133-120315183	LNCaP	prostate:	n/a
23	chr12:120315015-120315065	HUVEC	blood vessel:	n/a
24	chr12:120307689-120307739	HEK293	kidney:	embryo
25	chr12:120315283-120315333	HNPCEpiC	eye:	n/a
26	chr12:120315422-120315472	AG10803	skin:	n/a
27	chr12:120314679-120314729	PANC-1	pancreas:	n/a
28	chr12:120317798-120317848	GM12891	blood:	n/a
29	chr12:120315015-120315065	Hepatocyte	liver:	n/a
30	chr12:120315368-120315418	RPTEC	kidney:	n/a
31	chr12:120315422-120315472	SK-N-SH_RA	brain:	n/a
32	chr12:120315162-120315212	HCF	heart:	n/a
33	chr12:120314679-120314729	SKMC	muscle:	n/a
34	chr12:120315162-120315212	CMK	blood:	n/a
35	chr12:120315162-120315212	LNCaP	prostate:	n/a
36	chr12:120313949-120313999	PANC-1	pancreas:	n/a
37	chr12:120315015-120315065	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:120315368-120315418	HepG2	liver:	n/a
39	chr12:120315168-120315218	SAEC	small airway:	n/a
40	chr12:120315144-120315194	BE2_C	brain:	n/a
41	chr12:120315669-120315719	LNCaP	prostate:	n/a
42	chr12:120315422-120315472	AG09319	gingival:	n/a
43	chr12:120314679-120314729	HIPEpiC	eye:	n/a
44	chr12:120315144-120315194	AG04450	lung:	fetal
45	chr12:120315368-120315418	H1-hESC	embryonic stem cell:	embryo
46	chr12:120307689-120307739	HRE	kidney:	n/a
47	chr12:120315133-120315183	Jurkat	blood:	n/a
48	chr12:120315368-120315418	NB4	blood:	n/a
49	chr12:120317798-120317848	HNPCEpiC	eye:	n/a
50	chr12:120317798-120317848	T-47D	breast:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:120375923..120377476-chr12:120425555..120428485,2	MCF-7	breast:
2	chr12:120419275..120421989-chr12:120429002..120431271,2	K562	blood:
3	chr12:120302511..120304719-chr12:120314276..120316054,2	MCF-7	breast:
4	chr12:120315180..120318058-chr12:120425281..120427733,2	K562	blood:
5	chr12:120410200..120412264-chr12:120425833..120427845,2	MCF-7	breast:
6	chr12:120260751..120262448-chr12:120266066..120268905,2	K562	blood:
7	chr12:120378947..120381276-chr12:120381985..120383684,2	MCF-7	breast:
8	chr12:120264164..120265852-chr12:120268752..120270479,2	MCF-7	breast:
9	chr12:120378824..120381346-chr12:120729788..120731312,2	MCF-7	breast:
10	chr12:120313396..120316395-chr17:41464679..41467181,3	MCF-7	breast:
11	chr12:120306038..120308979-chr12:120311898..120314369,2	MCF-7	breast:
12	chr12:120302541..120304201-chr12:120307024..120309528,2	MCF-7	breast:
13	chr12:120256458..120258729-chr12:120260465..120262298,2	K562	blood:
14	chr12:120410929..120415600-chr12:120416913..120420697,4	MCF-7	breast:
15	chr12:120264164..120265852-chr12:120268752..120270479,2	MCF-7	breast:
16	chr12:120364509..120367078-chr12:120552925..120555648,3	MCF-7	breast:
17	chr12:120331860..120334916-chr12:120338712..120341359,3	K562	blood:
18	chr12:120271067..120273765-chr12:120347314..120349886,2	K562	blood:
19	chr12:120294026..120296847-chr12:120307965..120310392,2	MCF-7	breast:
20	chr12:120420153..120423656-chr12:120424541..120427660,4	MCF-7	breast:
21	chr12:120419269..120420900-chr12:120635417..120637963,2	MCF-7	breast:
22	chr12:120259219..120262251-chr12:120264646..120267569,3	K562	blood:
23	chr12:120378840..120380961-chr12:120385159..120388054,2	MCF-7	breast:
24	chr12:120339915..120340470-chr20:52195293..52195889,2	MCF-7	breast:
25	chr12:120376974..120380203-chr12:120515998..120518791,3	MCF-7	breast:
26	chr12:120311757..120313490-chr12:120315922..120318216,2	K562	blood:
27	chr12:120298087..120299763-chr12:120301664..120303346,2	MCF-7	breast:
28	chr12:120410711..120413319-chr12:120426035..120428974,2	MCF-7	breast:
29	chr12:120340057..120342640-chr12:120728214..120730004,2	K562	blood:
30	chr12:120352684..120354311-chr12:120553510..120556280,2	MCF-7	breast:
31	chr12:120302350..120306271-chr12:120306775..120309464,5	K562	blood:
32	chr12:120332998..120334916-chr12:120338712..120340934,2	K562	blood:
33	chr12:120264314..120266239-chr12:120268781..120271075,2	K562	blood:
34	chr12:120255241..120258410-chr12:120258603..120261965,3	K562	blood:
35	chr12:120260854..120262430-chr12:120271416..120273361,2	K562	blood:
36	chr12:120264314..120266239-chr12:120268781..120271075,2	K562	blood:
37	chr12:120306038..120308979-chr12:120311898..120314369,2	MCF-7	breast:
38	chr12:120241999..120242594-chr12:120272678..120273440,2	MCF-7	breast:
39	chr12:120347765..120349996-chr12:120352909..120355244,2	MCF-7	breast:
40	chr12:120274242..120277869-chr12:120277898..120281203,3	K562	blood:
41	chr12:120260854..120262430-chr12:120271416..120273361,2	K562	blood:
42	chr12:120259219..120262251-chr12:120264646..120267569,3	K562	blood:
43	chr12:120378947..120381276-chr12:120381985..120383684,2	MCF-7	breast:
44	chr12:120271067..120273765-chr12:120347314..120349886,2	K562	blood:
45	chr12:120347765..120349996-chr12:120352909..120355244,2	MCF-7	breast:
46	chr12:120120248..120122666-chr12:120276652..120278749,2	K562	blood:
47	chr12:120375794..120377491-chr12:120554770..120557327,2	MCF-7	breast:
48	chr12:120410929..120415600-chr12:120416913..120420697,4	MCF-7	breast:
49	chr12:120313415..120316416-chr17:41464359..41467641,4	K562	blood:
50	chr12:120260751..120262448-chr12:120266066..120268905,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCDC64-2	chr12:120377270-120377404	NONHSAT031098
2	lnc-CCDC64-3	chr12:120351754-120351991	expRegAs_chr12_11307_+
3	lnc-CCDC64-2	chr12:120412822-120412950	NONHSAT031098

No data

Variant related genes	Relation type
RPL35AP30	TF binding region
CIT	TF binding region
RPL35AP30	CpG island
CIT	CpG island
ENSG00000111737	chromatin interactions
ENSG00000122966	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000260035	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000138606	chromatin interactions
ENSG00000226729	chromatin interactions
ENSG00000135127	chromatin interactions
ENSG00000255857	chromatin interactions
ENSG00000168175	chromatin interactions
ENSG00000122034	chromatin interactions
ENSG00000089157	chromatin interactions

Extended variants
information (count: 4164 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4164 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4767848	chr12:120259679-120259680	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538550354	chr12:120259694-120259695	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576820123	chr12:120259712-120259713	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376666739	chr12:120259779-120259780	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565521393	chr12:120259783-120259784	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534430850	chr12:120259838-120259839	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554206740	chr12:120259895-120259896	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537205741	chr12:120259896-120259897	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573904417	chr12:120259923-120259924	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10507289	chr12:120259924-120259925	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556475917	chr12:120259932-120259933	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576713388	chr12:120259951-120259952	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139285718	chr12:120260007-120260008	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558032145	chr12:120260020-120260021	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368383978	chr12:120260029-120260030	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527652030	chr12:120260080-120260081	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573377391	chr12:120260103-120260104	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149984458	chr12:120260172-120260173	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561319763	chr12:120260251-120260252	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146561046	chr12:120260341-120260342	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549990440	chr12:120260358-120260359	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs557111997	chr12:120260396-120260397	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569737846	chr12:120260401-120260402	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186627787	chr12:120260418-120260419	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552162905	chr12:120260442-120260443	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141208450	chr12:120260515-120260516	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540596087	chr12:120260523-120260524	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79086492	chr12:120260541-120260542	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554245260	chr12:120260567-120260568	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567860375	chr12:120260595-120260596	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536738117	chr12:120260605-120260606	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190921205	chr12:120260607-120260608	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200303267	chr12:120260629-120260630	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199836387	chr12:120260663-120260664	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111714859	chr12:120260691-120260692	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149806257	chr12:120260704-120260705	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369209873	chr12:120260705-120260706	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145804827	chr12:120260706-120260707	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148991309	chr12:120260724-120260725	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373238484	chr12:120260760-120260761	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374942948	chr12:120260786-120260787	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572476140	chr12:120260795-120260796	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541485770	chr12:120260803-120260804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73418551	chr12:120260865-120260866	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs143522505	chr12:120260871-120260872	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369299052	chr12:120260872-120260873	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75930165	chr12:120260904-120260905	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs183064945	chr12:120260915-120260916	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188452843	chr12:120260928-120260929	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374275610	chr12:120260931-120260932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1409 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120209400-120293600	Weak transcription	Primary T cells from cord blood	blood
2	chr12:120223000-120314400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr12:120241600-120276600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr12:120242600-120259800	Weak transcription	NH-A	brain
5	chr12:120242600-120260200	Weak transcription	HUVEC	blood vessel
6	chr12:120242600-120276600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:120242600-120276800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr12:120242600-120279000	Weak transcription	Fetal Intestine Small	intestine
9	chr12:120242600-120279400	Weak transcription	Fetal Intestine Large	intestine
10	chr12:120242600-120293800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr12:120242600-120294400	Weak transcription	Fetal Kidney	kidney
12	chr12:120242800-120287800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr12:120243200-120288200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr12:120245200-120273000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr12:120245200-120276400	Weak transcription	Fetal Muscle Leg	muscle
16	chr12:120245600-120285200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr12:120247000-120274600	Weak transcription	HMEC	breast
18	chr12:120247200-120259800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr12:120247200-120274400	Weak transcription	NHEK	skin
20	chr12:120247200-120285800	Weak transcription	NHLF	lung
21	chr12:120247400-120264400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr12:120247400-120285800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr12:120247800-120272800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:120252000-120261600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr12:120253400-120266000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:120253600-120266800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr12:120253800-120259800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:120253800-120272400	Strong transcription	HUES64 Cell Line	embryonic stem cell
29	chr12:120254000-120261200	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr12:120254800-120286400	Weak transcription	Fetal Muscle Trunk	muscle
31	chr12:120254800-120314600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr12:120255800-120264600	Weak transcription	Osteobl	bone
33	chr12:120256000-120261200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
34	chr12:120256400-120263000	Weak transcription	Hela-S3	cervix
35	chr12:120256600-120268400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:120256600-120304000	Weak transcription	Fetal Heart	heart
37	chr12:120256800-120260000	Weak transcription	HSMM	muscle
38	chr12:120257200-120259800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr12:120257200-120260000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr12:120257200-120260200	Weak transcription	Primary hematopoietic stem cells	blood
41	chr12:120257200-120265800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr12:120257200-120270400	Weak transcription	Fetal Stomach	stomach
43	chr12:120257400-120259800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr12:120257400-120263000	Weak transcription	GM12878-XiMat	blood
45	chr12:120257400-120277800	Weak transcription	Fetal Brain Female	brain
46	chr12:120257800-120260400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr12:120257800-120263000	Weak transcription	Thymus	Thymus
48	chr12:120257800-120270400	Weak transcription	HepG2	liver
49	chr12:120257800-120275000	Weak transcription	K562	blood
50	chr12:120258000-120259800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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