Variant report

Variant	nsv832771
Chromosome Location	chr14:36771007-36964041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1473)
CpG islands
(count:672)
Chromatin interactive
region (count:77)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1473 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:36784635-36784815	K562	blood:	n/a	n/a
2	ARID3A	chr14:36789827-36789998	K562	blood:	n/a	n/a
3	ARID3A	chr14:36786874-36787050	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:36789353-36790203	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:36787931-36788470	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:36785526-36785702	K562	blood:	n/a	n/a
7	ATF1	chr14:36789684-36790159	K562	blood:	n/a	n/a
8	ATF2	chr14:36789725-36790108	GM12878	blood:	n/a	n/a
9	ATF2	chr14:36789693-36790117	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr14:36789612-36790132	GM12878	blood:	n/a	n/a
11	ATF3	chr14:36789354-36790107	HepG2	liver:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
12	ATF3	chr14:36789736-36790012	K562	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
13	ATF3	chr14:36789635-36790064	H1-hESC	embryonic stem cell:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
14	ATF3	chr14:36789765-36789985	GM12878	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
15	BACH1	chr14:36909902-36910233	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr14:36919142-36919480	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr14:36830734-36830922	K562	blood:	n/a	n/a
18	BACH1	chr14:36862356-36862387	K562	blood:	n/a	n/a
19	BACH1	chr14:36922214-36922350	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr14:36912121-36912783	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr14:36947950-36948249	GM12878	blood:	n/a	chr14:36948069-36948079 chr14:36948068-36948079
22	BATF	chr14:36784705-36785059	GM12878	blood:	n/a	chr14:36784842-36784853
23	BATF	chr14:36947908-36948298	GM12878	blood:	n/a	chr14:36948069-36948079 chr14:36948068-36948079
24	BATF	chr14:36784726-36785054	GM12878	blood:	n/a	chr14:36784842-36784853
25	BATF	chr14:36948604-36948948	GM12878	blood:	n/a	chr14:36948741-36948752
26	BCL3	chr14:36784682-36784987	GM12878	blood:	n/a	chr14:36784811-36784820
27	BCL3	chr14:36922457-36922825	GM12878	blood:	n/a	n/a
28	BCL3	chr14:36937823-36938143	GM12878	blood:	n/a	n/a
29	BCL3	chr14:36789549-36790347	A549	lung:	n/a	n/a
30	BHLHE40	chr14:36784748-36785137	GM12878	blood:	n/a	n/a
31	BHLHE40	chr14:36789595-36790169	K562	blood:	n/a	n/a
32	BHLHE40	chr14:36843205-36843569	K562	blood:	n/a	n/a
33	BRCA1	chr14:36843310-36843576	HepG2	liver:	n/a	n/a
34	BRCA1	chr14:36788746-36788783	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr14:36789033-36790188	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr14:36789668-36790245	HepG2	liver:	n/a	n/a
37	CBX3	chr14:36789680-36790403	K562	blood:	n/a	n/a
38	CBX3	chr14:36843125-36843683	HCT-116	colon:	n/a	n/a
39	CBX3	chr14:36826125-36826377	K562	blood:	n/a	n/a
40	CBX3	chr14:36826062-36826365	K562	blood:	n/a	n/a
41	CCNT2	chr14:36789394-36790044	K562	blood:	n/a	chr14:36789846-36789855
42	CEBPB	chr14:36796651-36796792	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr14:36789746-36790117	K562	blood:	n/a	n/a
44	CEBPB	chr14:36874463-36874761	HepG2	liver:	n/a	chr14:36874627-36874638 chr14:36874566-36874579 chr14:36874567-36874578
45	CEBPB	chr14:36789706-36790106	HepG2	liver:	n/a	n/a
46	CEBPB	chr14:36789331-36790233	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr14:36832879-36833223	Hela-S3	cervix:	n/a	chr14:36833053-36833066 chr14:36833054-36833065
48	CEBPB	chr14:36796572-36796924	A549	lung:	n/a	n/a
49	CEBPB	chr14:36903308-36903511	HepG2	liver:	n/a	chr14:36903313-36903326 chr14:36903460-36903471
50	CEBPB	chr14:36893954-36894236	ECC-1	luminal epithelium:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36789691-36789741	GM19239	blood:	n/a
2	chr14:36789691-36789741	GM19239	blood:	n/a
3	chr14:36783435-36783485	BJ	skin:	n/a
4	chr14:36789985-36790035	AG09319	gingival:	n/a
5	chr14:36789886-36789936	HRCEpiC	kidney:	n/a
6	chr14:36789691-36789741	MCF10A-Er-Src	breast:	n/a
7	chr14:36789810-36789860	ovcar-3	ovarian:	n/a
8	chr14:36789886-36789936	Jurkat	blood:	n/a
9	chr14:36910311-36910361	AG09319	gingival:	n/a
10	chr14:36899948-36899998	HCM	heart:	n/a
11	chr14:36892906-36892956	AG10803	skin:	n/a
12	chr14:36789810-36789860	HCF	heart:	n/a
13	chr14:36790242-36790292	AG04449	skin:	fetal
14	chr14:36789691-36789741	MCF-7	breast:	n/a
15	chr14:36942999-36943049	HEEpiC	esophagus:	n/a
16	chr14:36789886-36789936	HEK293	kidney:	embryo
17	chr14:36789488-36789538	HMEC	breast:	n/a
18	chr14:36789985-36790035	RPTEC	kidney:	n/a
19	chr14:36899948-36899998	NT2-D1	testis:	n/a
20	chr14:36789488-36789538	BE2_C	brain:	n/a
21	chr14:36789488-36789538	SK-N-SH_RA	brain:	n/a
22	chr14:36899948-36899998	Hela-S3	cervix:	n/a
23	chr14:36942999-36943049	RPTEC	kidney:	n/a
24	chr14:36899948-36899998	HMEC	breast:	n/a
25	chr14:36789691-36789741	AG04450	lung:	fetal
26	chr14:36789810-36789860	NT2-D1	testis:	n/a
27	chr14:36789886-36789936	MCF10A-Er-Src	breast:	n/a
28	chr14:36783435-36783485	AG10803	skin:	n/a
29	chr14:36892906-36892956	AG04450	lung:	fetal
30	chr14:36789488-36789538	HEK293	kidney:	embryo
31	chr14:36789985-36790035	HMEC	breast:	n/a
32	chr14:36789488-36789538	SK-N-SH	brain:	n/a
33	chr14:36789985-36790035	BE2_C	brain:	n/a
34	chr14:36789691-36789741	ECC-1	luminal epithelium:	n/a
35	chr14:36942999-36943049	LNCaP	prostate:	n/a
36	chr14:36892906-36892956	NHDF-neo	bronchial:	n/a
37	chr14:36790242-36790292	HUVEC	blood vessel:	n/a
38	chr14:36910311-36910361	NHBE	bronchial:	n/a
39	chr14:36783435-36783485	HCPEpiC	choroid plexus:	n/a
40	chr14:36789488-36789538	NT2-D1	testis:	n/a
41	chr14:36789488-36789538	AG09309	skin:	n/a
42	chr14:36942999-36943049	PFSK-1	brain:	n/a
43	chr14:36910311-36910361	SKMC	muscle:	n/a
44	chr14:36789691-36789741	HRE	kidney:	n/a
45	chr14:36789810-36789860	NHBE	bronchial:	n/a
46	chr14:36783435-36783485	AG04450	lung:	fetal
47	chr14:36899948-36899998	NB4	blood:	n/a
48	chr14:36789691-36789741	NHBE	bronchial:	n/a
49	chr14:36942999-36943049	AG09319	gingival:	n/a
50	chr14:36899948-36899998	AG09319	gingival:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:36574215..36575079-chr14:36842954..36843910,3	MCF-7	breast:
2	chr14:36539372..36539907-chr14:36843034..36843796,2	K562	blood:
3	chr14:36872054..36873602-chr14:36876368..36878600,2	K562	blood:
4	chr14:36918851..36919626-chr14:37586517..37587298,2	MCF-7	breast:
5	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
6	chr14:36953506..36955030-chr14:36956461..36958948,2	K562	blood:
7	chr14:36539398..36539927-chr14:36782854..36783534,2	MCF-7	breast:
8	chr1:53308102..53308983-chr14:36776394..36777212,2	MCF-7	breast:
9	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
10	chr14:36780690..36783423-chr14:36785409..36787697,2	K562	blood:
11	chr14:36829103..36831053-chr14:36832604..36834528,2	MCF-7	breast:
12	chr14:36943634..36946516-chr14:36949128..36951059,2	K562	blood:
13	chr14:36539344..36540319-chr14:36843032..36843752,3	MCF-7	breast:
14	chr14:36784077..36786059-chr14:36788034..36791140,4	MCF-7	breast:
15	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
16	chr14:36953506..36955030-chr14:36956461..36958948,2	K562	blood:
17	chr14:36784989..36787450-chr14:36787865..36790918,4	K562	blood:
18	chr14:36834496..36836870-chr14:36873397..36875476,2	MCF-7	breast:
19	chr14:36774640..36776851-chr14:36779144..36781211,2	K562	blood:
20	chr14:36847892..36849551-chr14:36851800..36853748,2	MCF-7	breast:
21	chr14:36676468..36677430-chr14:36842915..36843825,2	MCF-7	breast:
22	chr14:36888946..36890846-chr14:36890919..36892616,2	K562	blood:
23	chr14:36830141..36832538-chr14:36833542..36835967,2	K562	blood:
24	chr14:36919115..36919786-chr14:36989463..36990387,3	MCF-7	breast:
25	chr14:36952546..36954058-chr14:36970289..36971899,2	K562	blood:
26	chr14:36830381..36833257-chr14:36835947..36837458,2	MCF-7	breast:
27	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
28	chr14:36676675..36678036-chr14:36919496..36920913,3	MCF-7	breast:
29	chr14:36778847..36780826-chr14:36784208..36786054,2	MCF-7	breast:
30	chr14:36774640..36777657-chr14:36778032..36780826,3	K562	blood:
31	chr14:36943634..36946516-chr14:36949128..36951059,2	K562	blood:
32	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
33	chr14:36918758..36921054-chr14:37025630..37028183,2	MCF-7	breast:
34	chr14:36710205..36711140-chr14:36919414..36920201,2	MCF-7	breast:
35	chr14:36918997..36920049-chr14:37073904..37074754,4	MCF-7	breast:
36	chr14:36842718..36843503-chr19:10784986..10785706,2	MCF-7	breast:
37	chr14:36918821..36920421-chr14:36994175..36995365,7	MCF-7	breast:
38	chr14:36939446..36942264-chr14:36943575..36946382,2	K562	blood:
39	chr14:36710168..36711061-chr14:36843146..36843702,2	MCF-7	breast:
40	chr14:36918670..36920976-chr14:36921405..36923401,2	MCF-7	breast:
41	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
42	chr14:36919935..36920446-chr14:36994636..36995297,2	MCF-7	breast:
43	chr14:36777645..36780229-chr14:36786756..36790572,4	MCF-7	breast:
44	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
45	chr14:36914655..36916948-chr14:36920677..36922578,2	MCF-7	breast:
46	chr14:36872054..36873602-chr14:36876368..36878600,2	K562	blood:
47	chr14:36919018..36919802-chr14:37025877..37026711,2	MCF-7	breast:
48	chr14:36918670..36920976-chr14:36921405..36923401,2	MCF-7	breast:
49	chr14:36538483..36541249-chr14:36788541..36791272,2	MCF-7	breast:
50	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAX9-10	chr14:36785664-36785887	uc_374_+
2	lnc-PAX9-9	chr14:36840370-36841574	NONHSAT036431
3	lnc-SFTA3-2	chr14:36785664-36785887	uc_374_-
4	lnc-SFTA3-1	chr14:36942412-36943086	ENSG00000257520.1
5	lnc-SFTA3-1	chr14:36946174-36947171	NONHSAT036437
6	lnc-SFTA3-1	chr14:36960406-36960496	ENSG00000257520.1
7	lnc-SFTA3-1	chr14:36960406-36960496	NONHSAT036438
8	lnc-PAX9-5	chr14:36930958-36931266	XLOC_010800
9	lnc-PAX9-9	chr14:36840370-36841588	NONHSAT036430
10	lnc-SFTA3-1	chr14:36943875-36944078	NONHSAT036437
11	lnc-SFTA3-1	chr14:36943883-36944078	NONHSAT036438
12	lnc-SFTA3-1	chr14:36946744-36946833	NONHSAT036439
13	lnc-SFTA3-1	chr14:36946176-36946308	ENSG00000257520.1
14	lnc-SFTA3-1	chr14:36946921-36947083	ENSG00000257520.1
15	lnc-SFTA3-1	chr14:36946506-36946646	NONHSAT036439
16	lnc-SFTA3-1	chr14:36946224-36946308	NONHSAT036439
17	lnc-PAX9-5	chr14:36931376-36931579	XLOC_010800
18	lnc-SFTA3-1	chr14:36942493-36943086	NONHSAT036437

No data

Variant related genes	Relation type
SFTA3	TF binding region
DPPA3P2	TF binding region
MBIP	TF binding region
RNU7-93P	TF binding region
SFTA3	CpG island
DPPA3P2	CpG island
MBIP	CpG island
RNU7-93P	CpG island
ENSG00000182197	chromatin interactions
ENSG00000203995	chromatin interactions
ENSG00000136352	chromatin interactions
ENSG00000151332	chromatin interactions
ENSG00000257585	chromatin interactions
ENSG00000238540	chromatin interactions

Extended variants
information (count: 3927 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3927 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551744952	chr14:36771048-36771049	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571427762	chr14:36771146-36771147	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533815665	chr14:36771167-36771168	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553502141	chr14:36771201-36771202	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368712687	chr14:36771242-36771243	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567225240	chr14:36771332-36771333	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535967993	chr14:36771336-36771337	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374491724	chr14:36771404-36771405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371792892	chr14:36771469-36771470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529115195	chr14:36771585-36771586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376166637	chr14:36771622-36771623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545175341	chr14:36771623-36771624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558858229	chr14:36771629-36771630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572665858	chr14:36771638-36771639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370755798	chr14:36771654-36771655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs561130808	chr14:36771672-36771673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530066776	chr14:36771694-36771695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560901777	chr14:36771698-36771699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs61994979	chr14:36771728-36771729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372709968	chr14:36771745-36771746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543977220	chr14:36771808-36771809	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375191110	chr14:36771844-36771845	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192329468	chr14:36771891-36771892	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140976284	chr14:36771924-36771925	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs17104334	chr14:36771939-36771940	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs528062710	chr14:36771965-36771966	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs527611985	chr14:36771996-36771997	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs34234768	chr14:36772019-36772020	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs144993785	chr14:36772033-36772034	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs567158443	chr14:36772054-36772055	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs535834947	chr14:36772056-36772057	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs146774670	chr14:36772058-36772059	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs184540614	chr14:36772064-36772065	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs555869000	chr14:36772081-36772082	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs569397269	chr14:36772088-36772089	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs538312482	chr14:36772126-36772127	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs7140630	chr14:36772184-36772185	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs572555755	chr14:36772219-36772220	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs188942558	chr14:36772269-36772270	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs117308137	chr14:36772283-36772284	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs574789404	chr14:36772356-36772357	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs140500735	chr14:36772404-36772405	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs117998357	chr14:36772412-36772413	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs577428682	chr14:36772452-36772453	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs192752735	chr14:36772467-36772468	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs116603958	chr14:36772488-36772489	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs116336360	chr14:36772494-36772495	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs547415100	chr14:36772496-36772497	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561231479	chr14:36772524-36772525	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs7141354	chr14:36772564-36772565	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD

Chromatin state (count:1297 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36761000-36785000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:36762000-36778800	Weak transcription	Fetal Intestine Small	intestine
3	chr14:36763800-36777800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr14:36764400-36784000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr14:36765000-36779400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr14:36765000-36781200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr14:36765200-36781400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr14:36765400-36773000	Strong transcription	Fetal Brain Female	brain
9	chr14:36765400-36775200	Strong transcription	Adipose Nuclei	Adipose
10	chr14:36765400-36781400	Strong transcription	Placenta	Placenta
11	chr14:36765400-36788800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr14:36765600-36781000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:36765800-36771200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr14:36765800-36772000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr14:36765800-36775600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr14:36765800-36776400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr14:36765800-36780000	Weak transcription	K562	blood
18	chr14:36765800-36781000	Strong transcription	Duodenum Mucosa	Duodenum
19	chr14:36765800-36781200	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr14:36765800-36782200	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr14:36766000-36775200	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr14:36766000-36777800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr14:36766000-36781000	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr14:36766000-36781000	Strong transcription	Skeletal Muscle Female	skeletal muscle
25	chr14:36766000-36781400	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr14:36766000-36783400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr14:36766200-36772200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:36766200-36778000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr14:36766200-36781200	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr14:36766200-36781200	Strong transcription	Fetal Thymus	thymus
31	chr14:36766200-36781200	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr14:36766200-36781400	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr14:36766200-36785400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr14:36766400-36779200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr14:36766600-36788000	Weak transcription	Fetal Heart	heart
36	chr14:36766800-36779600	Weak transcription	Right Ventricle	heart
37	chr14:36767000-36772000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr14:36767000-36781000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:36767000-36781400	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr14:36767200-36772600	Weak transcription	Esophagus	oesophagus
41	chr14:36767200-36779400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr14:36767400-36772000	Weak transcription	Left Ventricle	heart
43	chr14:36767400-36772000	Weak transcription	Pancreas	Pancrea
44	chr14:36767400-36772800	Weak transcription	Small Intestine	intestine
45	chr14:36767400-36778000	Weak transcription	Thymus	Thymus
46	chr14:36767400-36778200	Weak transcription	Lung	lung
47	chr14:36767400-36789200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr14:36767400-36789200	Weak transcription	Spleen	Spleen
49	chr14:36767600-36772000	Weak transcription	Brain Cingulate Gyrus	brain
50	chr14:36767600-36778200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links