Variant report

Variant	nsv899490
Chromosome Location	chr12:104149022-104218956
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1100)
CpG islands
(count:488)
Chromatin interactive
region (count:97)
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	chr12:104193782-104194213	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:104179242-104179647	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:104165372-104165467	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:104202957-104203376	K562	blood:	n/a	n/a
5	ARID3A	chr12:104193999-104194315	K562	blood:	n/a	n/a
6	ARID3A	chr12:104198820-104199164	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:104198755-104199383	K562	blood:	n/a	n/a
8	ATF1	chr12:104198800-104199070	K562	blood:	n/a	n/a
9	ATF3	chr12:104199243-104199393	K562	blood:	n/a	n/a
10	ATF3	chr12:104198713-104199538	K562	blood:	n/a	n/a
11	ATF3	chr12:104198693-104199416	A549	lung:	n/a	n/a
12	BATF	chr12:104198692-104199049	GM12878	blood:	n/a	chr12:104198872-104198883
13	BATF	chr12:104198779-104198976	GM12878	blood:	n/a	chr12:104198872-104198883
14	BCL3	chr12:104193441-104194009	A549	lung:	n/a	n/a
15	BCL3	chr12:104193398-104193993	A549	lung:	n/a	n/a
16	BHLHE40	chr12:104165289-104165416	K562	blood:	n/a	n/a
17	BHLHE40	chr12:104202911-104203339	K562	blood:	n/a	n/a
18	BHLHE40	chr12:104194009-104194255	K562	blood:	n/a	n/a
19	BHLHE40	chr12:104198806-104199084	K562	blood:	n/a	n/a
20	BRCA1	chr12:104211055-104211057	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr12:104198806-104199226	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr12:104193428-104194312	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr12:104198664-104199701	K562	blood:	n/a	n/a
24	CBX3	chr12:104202819-104203880	K562	blood:	n/a	n/a
25	CBX3	chr12:104206584-104206897	K562	blood:	n/a	n/a
26	CBX3	chr12:104198693-104199438	HCT-116	colon:	n/a	n/a
27	CBX3	chr12:104198658-104199180	HCT-116	colon:	n/a	n/a
28	CCNT2	chr12:104198848-104199366	K562	blood:	n/a	n/a
29	CCNT2	chr12:104193958-104194301	K562	blood:	n/a	n/a
30	CCNT2	chr12:104202960-104203361	K562	blood:	n/a	chr12:104203091-104203111
31	CEBPB	chr12:104193379-104194081	HCT-116	colon:	n/a	n/a
32	CEBPB	chr12:104179129-104179274	HepG2	liver:	n/a	chr12:104179214-104179225
33	CEBPB	chr12:104198711-104199517	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr12:104174023-104174310	A549	lung:	n/a	n/a
35	CEBPB	chr12:104200562-104200758	K562	blood:	n/a	n/a
36	CEBPB	chr12:104193274-104194350	A549	lung:	n/a	n/a
37	CEBPB	chr12:104193532-104193872	HepG2	liver:	n/a	n/a
38	CEBPB	chr12:104195613-104196307	IMR90	lung:	n/a	n/a
39	CEBPB	chr12:104193581-104193896	K562	blood:	n/a	n/a
40	CEBPB	chr12:104193356-104193959	HepG2	liver:	n/a	n/a
41	CEBPB	chr12:104193585-104194167	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr12:104198794-104199080	K562	blood:	n/a	n/a
43	CEBPB	chr12:104218672-104219010	IMR90	lung:	n/a	n/a
44	CEBPB	chr12:104193576-104193947	HepG2	liver:	n/a	n/a
45	CEBPB	chr12:104179122-104179394	HepG2	liver:	n/a	chr12:104179214-104179225
46	CEBPB	chr12:104193458-104194199	K562	blood:	n/a	n/a
47	CEBPB	chr12:104193475-104194087	MCF-7	breast:	n/a	n/a
48	CEBPB	chr12:104193407-104194152	MCF-7	breast:	n/a	n/a
49	CEBPB	chr12:104193583-104193967	K562	blood:	n/a	n/a
50	CEBPB	chr12:104193557-104193979	IMR90	lung:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:104195610-104195660	SK-N-MC	brain:	n/a
2	chr12:104178138-104178188	HRPEpiC	eye:	n/a
3	chr12:104178138-104178188	HL-60	blood:	n/a
4	chr12:104178138-104178188	PFSK-1	brain:	n/a
5	chr12:104178138-104178188	ovcar-3	ovarian:	n/a
6	chr12:104178138-104178188	NHBE	bronchial:	n/a
7	chr12:104218302-104218352	HPAEpiC	pulmonary alveolar:	n/a
8	chr12:104195610-104195660	Hepatocyte	liver:	n/a
9	chr12:104199610-104199660	SK-N-SH_RA	brain:	n/a
10	chr12:104178138-104178188	Jurkat	blood:	n/a
11	chr12:104173675-104173725	SK-N-SH_RA	brain:	n/a
12	chr12:104173675-104173725	BJ	skin:	n/a
13	chr12:104173675-104173725	AG10803	skin:	n/a
14	chr12:104218302-104218352	SAEC	small airway:	n/a
15	chr12:104163467-104163517	SAEC	small airway:	n/a
16	chr12:104199610-104199660	GM06990	blood:	n/a
17	chr12:104166357-104166407	HAEpiC	amniotic membrane:	n/a
18	chr12:104166357-104166407	HEK293	kidney:	embryo
19	chr12:104213449-104213499	AG10803	skin:	n/a
20	chr12:104178138-104178188	NH-A	brain:	n/a
21	chr12:104163467-104163517	HCF	heart:	n/a
22	chr12:104218302-104218352	HAEpiC	amniotic membrane:	n/a
23	chr12:104195610-104195660	ECC-1	luminal epithelium:	n/a
24	chr12:104218302-104218352	HL-60	blood:	n/a
25	chr12:104199610-104199660	NHDF-neo	bronchial:	n/a
26	chr12:104166357-104166407	LNCaP	prostate:	n/a
27	chr12:104199610-104199660	HL-60	blood:	n/a
28	chr12:104166357-104166407	HepG2	liver:	n/a
29	chr12:104173675-104173725	Jurkat	blood:	n/a
30	chr12:104199610-104199660	AG04449	skin:	fetal
31	chr12:104173675-104173725	LNCaP	prostate:	n/a
32	chr12:104218302-104218352	HNPCEpiC	eye:	n/a
33	chr12:104163467-104163517	GM06990	blood:	n/a
34	chr12:104178138-104178188	AoSMC	blood vessel:	n/a
35	chr12:104213449-104213499	PrEC	prostate:	n/a
36	chr12:104199610-104199660	HEK293	kidney:	embryo
37	chr12:104218302-104218352	HRCEpiC	kidney:	n/a
38	chr12:104163467-104163517	Hela-S3	cervix:	n/a
39	chr12:104199610-104199660	AG09309	skin:	n/a
40	chr12:104166357-104166407	HCPEpiC	choroid plexus:	n/a
41	chr12:104163467-104163517	NHDF-neo	bronchial:	n/a
42	chr12:104178138-104178188	HepG2	liver:	n/a
43	chr12:104213449-104213499	IMR90	lung:	fetal
44	chr12:104166357-104166407	Hela-S3	cervix:	n/a
45	chr12:104213449-104213499	NH-A	brain:	n/a
46	chr12:104195610-104195660	CMK	blood:	n/a
47	chr12:104173675-104173725	Caco-2	colon:	n/a
48	chr12:104173675-104173725	PANC-1	pancreas:	n/a
49	chr12:104173675-104173725	HIPEpiC	eye:	n/a
50	chr12:104195610-104195660	NHDF-neo	bronchial:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:104156601..104158304-chr12:104234434..104236510,2	MCF-7	breast:
2	chr12:104192025..104195229-chr12:104233820..104236988,3	K562	blood:
3	chr12:104181732..104183493-chr12:104185105..104187662,2	K562	blood:
4	chr12:104178636..104180567-chr12:104180995..104183516,2	K562	blood:
5	chr12:104195074..104198274-chr12:104203706..104206121,4	K562	blood:
6	chr12:104149022..104151249-chr12:104234261..104235961,2	MCF-7	breast:
7	chr12:104165050..104165668-chr12:104234645..104235407,2	MCF-7	breast:
8	chr12:104187183..104188924-chr12:104191126..104192831,2	K562	blood:
9	chr12:104166261..104169463-chr12:104174698..104177836,3	MCF-7	breast:
10	chr12:104206123..104208804-chr12:104221926..104227695,4	K562	blood:
11	chr12:104183971..104186585-chr12:104195377..104197351,2	MCF-7	breast:
12	chr12:104186150..104188258-chr12:104233575..104235121,2	K562	blood:
13	chr12:104166229..104169114-chr12:104169303..104172896,3	MCF-7	breast:
14	chr12:104194168..104195687-chr12:104197418..104199673,2	K562	blood:
15	chr12:104198469..104201339-chr12:104203097..104205273,3	MCF-7	breast:
16	chr12:104183990..104193430-chr12:104193641..104204611,16	MCF-7	breast:
17	chr12:104200580..104204661-chr12:104208067..104211223,3	K562	blood:
18	chr12:104199289..104201376-chr12:104228152..104230435,2	MCF-7	breast:
19	chr12:104171358..104174943-chr12:104233480..104236232,4	MCF-7	breast:
20	chr12:104166261..104169463-chr12:104174698..104177836,3	MCF-7	breast:
21	chr12:104198690..104201561-chr12:104203107..104206456,4	K562	blood:
22	chr12:104160749..104162806-chr12:104234443..104236279,2	MCF-7	breast:
23	chr12:104141190..104143680-chr12:104152511..104154434,2	MCF-7	breast:
24	chr12:104186877..104189949-chr12:104233437..104236104,3	MCF-7	breast:
25	chr12:104192326..104196273-chr12:104235179..104237558,3	K562	blood:
26	chr12:104192744..104195300-chr12:104227670..104230455,2	MCF-7	breast:
27	chr12:104198690..104200506-chr12:104204020..104206335,2	K562	blood:
28	chr12:104208479..104212455-chr12:104217163..104218930,3	MCF-7	breast:
29	chr12:104163207..104165311-chr12:104196733..104198239,2	K562	blood:
30	chr12:104215538..104217746-chr12:104226059..104228038,3	K562	blood:
31	chr12:104206137..104208857-chr12:104227836..104229349,2	K562	blood:
32	chr12:104183709..104186598-chr12:104189875..104192288,3	K562	blood:
33	chr12:104178670..104180428-chr12:104186156..104188204,2	K562	blood:
34	chr12:104183709..104186598-chr12:104189875..104192288,3	K562	blood:
35	chr12:104209730..104211808-chr12:104212200..104214278,2	K562	blood:
36	chr12:104177175..104180567-chr12:104180842..104183516,3	K562	blood:
37	chr12:104207300..104208804-chr12:104224699..104227695,2	K562	blood:
38	chr12:104186543..104188821-chr12:104190748..104192615,2	K562	blood:
39	chr12:104197681..104199804-chr12:104233310..104235105,2	K562	blood:
40	chr12:104214519..104222192-chr12:104231005..104236989,8	K562	blood:
41	chr12:104198918..104202818-chr12:104225755..104230550,5	K562	blood:
42	chr12:104176398..104178432-chr12:104233589..104235807,2	MCF-7	breast:
43	chr12:104208479..104212455-chr12:104217163..104218930,3	MCF-7	breast:
44	chr12:104177175..104180567-chr12:104180842..104183516,3	K562	blood:
45	chr12:104211319..104217420-chr12:104233507..104236073,8	MCF-7	breast:
46	chr12:104198690..104201561-chr12:104203107..104206456,4	K562	blood:
47	chr12:104166229..104169114-chr12:104169303..104172896,3	MCF-7	breast:
48	chr12:104190889..104195812-chr12:104232079..104236624,5	MCF-7	breast:
49	chr12:104156978..104159954-chr12:104162925..104164742,3	MCF-7	breast:
50	chr12:104164872..104166111-chr12:104264007..104265181,16	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-650K20.3.1-1	chr12:104213388-104213506	ENSG00000257754.1
2	lnc-NT5DC3-1	chr12:104157090-104157596	ENSG00000257681.1
3	lnc-NT5DC3-1	chr12:104160513-104160684	ENSG00000257681.1
4	lnc-RP11-650K20.3.1-1	chr12:104215642-104215863	ENSG00000257754.1
5	lnc-NT5DC3-1	chr12:104160513-104160691	ENSG00000257681.1
6	lnc-RP11-650K20.3.1-1	chr12:104214577-104214648	ENSG00000257754.1
7	lnc-NT5DC3-1	chr12:104162585-104162636	ENSG00000257681.1

No data

Variant related genes	Relation type
ENSG00000257681	TF binding region
ENSG00000257754	TF binding region
STAB2	TF binding region
NT5DC3	TF binding region
ENSG00000257681	CpG island
ENSG00000257754	CpG island
STAB2	CpG island
NT5DC3	CpG island
ENSG00000204954	chromatin interactions
ENSG00000136011	chromatin interactions
ENSG00000111696	chromatin interactions
ENSG00000257754	chromatin interactions
ENSG00000257327	chromatin interactions

Extended variants
information (count: 2846 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2846 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11111748	chr12:104149022-104149023	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374688619	chr12:104149122-104149123	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs367716332	chr12:104149145-104149146	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs147296184	chr12:104149146-104149147	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs200493377	chr12:104149205-104149206	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs201265382	chr12:104149212-104149213	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs34342881	chr12:104149229-104149230	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs375211716	chr12:104149232-104149233	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs369345696	chr12:104149236-104149237	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs147884936	chr12:104149237-104149238	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs201998394	chr12:104149246-104149247	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs7296626	chr12:104149251-104149252	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs35668920	chr12:104149264-104149265	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs201315467	chr12:104149279-104149280	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs560074533	chr12:104149309-104149310	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs61939566	chr12:104149315-104149316	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs577598597	chr12:104149318-104149319	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs374464895	chr12:104149357-104149358	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs537682838	chr12:104149406-104149407	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs561118556	chr12:104149434-104149435	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs140590853	chr12:104149445-104149446	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs141570058	chr12:104149466-104149467	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs34239451	chr12:104149471-104149472	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs377547432	chr12:104149483-104149484	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs7313163	chr12:104149520-104149521	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs375054106	chr12:104149522-104149523	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs149847796	chr12:104149531-104149532	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs559512311	chr12:104149535-104149536	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs145848240	chr12:104149542-104149543	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs7962758	chr12:104149559-104149560	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs551502032	chr12:104149561-104149562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs554470530	chr12:104149570-104149571	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs571411066	chr12:104149597-104149598	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs149012935	chr12:104149619-104149620	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs79021375	chr12:104149677-104149678	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs77265338	chr12:104149689-104149690	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs79553328	chr12:104149708-104149709	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143959374	chr12:104149793-104149794	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs191620116	chr12:104149853-104149854	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs4981022	chr12:104149874-104149875	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs549178043	chr12:104149881-104149882	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575376288	chr12:104149892-104149893	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs375232382	chr12:104149961-104149962	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs4981021	chr12:104149999-104150000	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs554978754	chr12:104150023-104150024	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs35585068	chr12:104150026-104150027	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs146426742	chr12:104150027-104150028	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs559638013	chr12:104150049-104150050	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs182656484	chr12:104150078-104150079	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs545263472	chr12:104150082-104150083	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	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
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2253 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104139200-104154200	Weak transcription	Rectal Smooth Muscle	rectum
2	chr12:104140600-104154600	Weak transcription	Aorta	Aorta
3	chr12:104142600-104152200	Weak transcription	HMEC	breast
4	chr12:104142800-104152000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:104142800-104154600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:104142800-104154600	Weak transcription	NHEK	skin
7	chr12:104143000-104149200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr12:104145400-104151400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:104145600-104154800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:104145800-104152000	Weak transcription	HSMMtube	muscle
11	chr12:104145800-104152400	Weak transcription	Esophagus	oesophagus
12	chr12:104145800-104166800	Weak transcription	Right Atrium	heart
13	chr12:104146000-104154600	Weak transcription	HSMM	muscle
14	chr12:104146200-104169400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr12:104146800-104150600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr12:104147000-104152200	Strong transcription	Spleen	Spleen
17	chr12:104147000-104159600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr12:104147000-104165400	Strong transcription	Stomach Smooth Muscle	stomach
19	chr12:104147400-104149200	Weak transcription	Liver	Liver
20	chr12:104147400-104151200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr12:104147400-104155800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr12:104148000-104154200	Weak transcription	Colon Smooth Muscle	Colon
23	chr12:104148200-104154400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr12:104148800-104152200	Weak transcription	Gastric	stomach
25	chr12:104149000-104149200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:104149000-104156800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr12:104149200-104149400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr12:104149200-104149400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:104149200-104149600	Strong transcription	Liver	Liver
30	chr12:104149200-104154200	Weak transcription	A549	lung
31	chr12:104149400-104149600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:104149400-104152200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr12:104149600-104151200	Weak transcription	Fetal Stomach	stomach
34	chr12:104149600-104151400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:104149600-104153800	Weak transcription	Liver	Liver
36	chr12:104150000-104156600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr12:104150000-104166800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr12:104150600-104151600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr12:104150600-104154200	Weak transcription	Placenta	Placenta
40	chr12:104150600-104155200	Weak transcription	Fetal Intestine Small	intestine
41	chr12:104151200-104153000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr12:104151200-104153200	Strong transcription	Fetal Stomach	stomach
43	chr12:104151400-104152600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:104151400-104152800	Enhancers	Fetal Muscle Trunk	muscle
45	chr12:104151400-104154800	Weak transcription	NH-A	brain
46	chr12:104151400-104158000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr12:104151600-104152200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr12:104151600-104152800	Enhancers	Fetal Muscle Leg	muscle
49	chr12:104151600-104152800	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr12:104151600-104155000	Weak transcription	Primary neutrophils fromperipheralblood	blood

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