Variant report

Variant	nsv906929
Chromosome Location	chr16:75569739-75594918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1010)
CpG islands
(count:977)
Chromatin interactive
region (count:73)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:75590112-75590226	K562	blood:	n/a	n/a
2	ARID3A	chr16:75593627-75593953	K562	blood:	n/a	n/a
3	ARID3A	chr16:75589106-75589336	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:75589058-75589467	K562	blood:	n/a	n/a
5	ATF1	chr16:75589062-75589521	K562	blood:	n/a	n/a
6	ATF2	chr16:75584173-75584552	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr16:75584143-75584635	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr16:75590084-75590537	GM12878	blood:	n/a	n/a
9	ATF3	chr16:75589109-75589551	K562	blood:	n/a	n/a
10	ATF3	chr16:75589061-75589505	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr16:75589247-75589391	K562	blood:	n/a	n/a
12	BACH1	chr16:75589143-75589515	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr16:75589994-75590043	K562	blood:	n/a	n/a
14	BCLAF1	chr16:75584089-75584523	GM12878	blood:	n/a	n/a
15	BCLAF1	chr16:75589572-75590518	GM12878	blood:	n/a	n/a
16	BCLAF1	chr16:75589106-75589503	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:75589800-75590343	GM12878	blood:	n/a	n/a
18	BHLHE40	chr16:75589135-75589414	K562	blood:	n/a	n/a
19	BHLHE40	chr16:75589725-75590355	K562	blood:	n/a	n/a
20	BHLHE40	chr16:75593964-75594273	K562	blood:	n/a	n/a
21	BRCA1	chr16:75588981-75589490	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr16:75593818-75594357	K562	blood:	n/a	n/a
23	CBX3	chr16:75588962-75590443	K562	blood:	n/a	n/a
24	CCNT2	chr16:75589293-75590420	K562	blood:	n/a	chr16:75589492-75589501 chr16:75590246-75590255
25	CEBPB	chr16:75590162-75590463	A549	lung:	n/a	n/a
26	CEBPB	chr16:75590207-75590346	HepG2	liver:	n/a	n/a
27	CEBPB	chr16:75580289-75580508	A549	lung:	n/a	chr16:75580396-75580407
28	CEBPB	chr16:75580259-75580553	HepG2	liver:	n/a	chr16:75580396-75580407
29	CEBPB	chr16:75589067-75589491	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr16:75580365-75580422	Hela-S3	cervix:	n/a	chr16:75580396-75580407
31	CEBPB	chr16:75581097-75581246	IMR90	lung:	n/a	n/a
32	CEBPB	chr16:75580234-75580559	K562	blood:	n/a	chr16:75580396-75580407
33	CEBPB	chr16:75590116-75590486	K562	blood:	n/a	n/a
34	CEBPB	chr16:75589035-75589434	IMR90	lung:	n/a	n/a
35	CEBPB	chr16:75581033-75581268	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:75589150-75589303	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:75584138-75584495	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr16:75580238-75580561	IMR90	lung:	n/a	chr16:75580396-75580407
39	CEBPB	chr16:75590077-75590412	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:75590156-75590452	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr16:75590087-75590490	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr16:75580237-75580534	H1-hESC	embryonic stem cell:	n/a	chr16:75580396-75580407
43	CEBPB	chr16:75581067-75581290	A549	lung:	n/a	n/a
44	CEBPB	chr16:75580218-75580505	MCF-7	breast:	n/a	chr16:75580396-75580407
45	CEBPB	chr16:75589141-75589383	K562	blood:	n/a	n/a
46	CHD1	chr16:75589820-75589996	GM12878	blood:	n/a	n/a
47	CHD1	chr16:75589003-75589482	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr16:75589079-75589235	GM12878	blood:	n/a	n/a
49	CHD1	chr16:75590452-75590544	GM12878	blood:	n/a	n/a
50	CHD2	chr16:75591056-75591161	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75572883-75572933	HepG2	liver:	n/a
2	chr16:75572883-75572933	HepG2	liver:	n/a
3	chr16:75590339-75590389	PANC-1	pancreas:	n/a
4	chr16:75593825-75593875	CMK	blood:	n/a
5	chr16:75590339-75590389	PFSK-1	brain:	n/a
6	chr16:75589561-75589611	HIPEpiC	eye:	n/a
7	chr16:75569852-75569902	PrEC	prostate:	n/a
8	chr16:75590339-75590389	A549	lung:	n/a
9	chr16:75593825-75593875	A549	lung:	n/a
10	chr16:75589572-75589622	AG09309	skin:	n/a
11	chr16:75593825-75593875	IMR90	lung:	fetal
12	chr16:75590184-75590234	A549	lung:	n/a
13	chr16:75590339-75590389	Hela-S3	cervix:	n/a
14	chr16:75587377-75587427	HMEC	breast:	n/a
15	chr16:75590170-75590220	MCF-7	breast:	n/a
16	chr16:75580831-75580881	HPAEpiC	pulmonary alveolar:	n/a
17	chr16:75590036-75590086	A549	lung:	n/a
18	chr16:75589467-75589517	AG09309	skin:	n/a
19	chr16:75590184-75590234	HL-60	blood:	n/a
20	chr16:75590184-75590234	PrEC	prostate:	n/a
21	chr16:75590170-75590220	AG09319	gingival:	n/a
22	chr16:75587377-75587427	HRE	kidney:	n/a
23	chr16:75593825-75593875	HNPCEpiC	eye:	n/a
24	chr16:75590339-75590389	RPTEC	kidney:	n/a
25	chr16:75589561-75589611	MCF-7	breast:	n/a
26	chr16:75569852-75569902	HAEpiC	amniotic membrane:	n/a
27	chr16:75589467-75589517	HRE	kidney:	n/a
28	chr16:75580831-75580881	HCF	heart:	n/a
29	chr16:75593825-75593875	GM12891	blood:	n/a
30	chr16:75575906-75575956	PrEC	prostate:	n/a
31	chr16:75590339-75590389	PrEC	prostate:	n/a
32	chr16:75589467-75589517	AG10803	skin:	n/a
33	chr16:75569852-75569902	NB4	blood:	n/a
34	chr16:75589561-75589611	NHDF-neo	bronchial:	n/a
35	chr16:75593825-75593875	Hela-S3	cervix:	n/a
36	chr16:75590309-75590359	MCF-7	breast:	n/a
37	chr16:75580831-75580881	CMK	blood:	n/a
38	chr16:75589467-75589517	HRCEpiC	kidney:	n/a
39	chr16:75590245-75590295	MCF10A-Er-Src	breast:	n/a
40	chr16:75575906-75575956	Hepatocyte	liver:	n/a
41	chr16:75589572-75589622	AG09319	gingival:	n/a
42	chr16:75590245-75590295	AoSMC	blood vessel:	n/a
43	chr16:75590170-75590220	HIPEpiC	eye:	n/a
44	chr16:75572883-75572933	GM12891	blood:	n/a
45	chr16:75590245-75590295	Hela-S3	cervix:	n/a
46	chr16:75580831-75580881	MCF-7	breast:	n/a
47	chr16:75575906-75575956	IMR90	lung:	fetal
48	chr16:75589561-75589611	SKMC	muscle:	n/a
49	chr16:75569852-75569902	GM12891	blood:	n/a
50	chr16:75589467-75589517	T-47D	breast:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:75533525..75534182-chr16:75573663..75574408,2	MCF-7	breast:
2	chr16:75496580..75498737-chr16:75588829..75590831,2	MCF-7	breast:
3	chr16:75587220..75591082-chr16:75591374..75595708,8	MCF-7	breast:
4	chr16:75584962..75586974-chr16:75587098..75590122,3	K562	blood:
5	chr16:75589583..75590159-chr3:42641596..42642441,2	Hela-S3	cervix:
6	chr16:75588861..75589599-chr5:43121516..43122217,2	Hela-S3	cervix:
7	chr16:75497024..75499172-chr16:75583005..75584978,2	MCF-7	breast:
8	chr16:75593028..75596412-chr16:75596623..75599848,3	MCF-7	breast:
9	chr16:75589604..75590145-chrX:23760858..23761653,2	Hela-S3	cervix:
10	chr16:75564501..75567219-chr16:75571368..75573194,2	K562	blood:
11	chr16:75568229..75570112-chr16:75587872..75589519,2	K562	blood:
12	chr16:75593216..75596661-chr16:75599139..75601757,3	MCF-7	breast:
13	chr16:75231754..75233579-chr16:75584595..75587243,2	MCF-7	breast:
14	chr15:65133627..65134289-chr16:75589695..75590232,2	Hela-S3	cervix:
15	chr16:75549961..75554189-chr16:75589462..75592660,4	K562	blood:
16	chr16:75589199..75589917-chr5:89705066..89705816,2	Hela-S3	cervix:
17	chr16:75572249..75573874-chr16:75680228..75682477,2	MCF-7	breast:
18	chr16:75583064..75584651-chr16:75587714..75590020,2	K562	blood:
19	chr16:75539405..75540962-chr16:75572342..75574110,2	K562	blood:
20	chr16:75586208..75590870-chr16:75596068..75600585,8	K562	blood:
21	chr16:75555207..75556271-chr16:75583820..75584762,4	MCF-7	breast:
22	chr16:75555425..75555952-chr16:75584155..75584681,2	MCF-7	breast:
23	chr16:75549686..75552508-chr16:75588605..75590350,2	MCF-7	breast:
24	chr16:75570762..75572723-chr16:75573865..75576124,2	K562	blood:
25	chr16:75589355..75592242-chr16:75608320..75611115,2	K562	blood:
26	chr16:75576612..75578705-chr16:75660423..75663143,2	K562	blood:
27	chr16:75587953..75591056-chr16:75597056..75601894,6	MCF-7	breast:
28	chr16:75589724..75591808-chr16:75655719..75657999,2	MCF-7	breast:
29	chr16:75574449..75576989-chr16:75588011..75589806,2	K562	blood:
30	chr16:75594188..75595805-chr16:75596164..75598150,2	K562	blood:
31	chr16:75589388..75590260-chr6:27860868..27861371,2	Hela-S3	cervix:
32	chr16:75580825..75584204-chr16:75588624..75590540,3	MCF-7	breast:
33	chr16:75574262..75576234-chr16:75588612..75590836,2	MCF-7	breast:
34	chr16:75589928..75591467-chr16:75655261..75657250,2	K562	blood:
35	chr16:75583056..75585935-chr16:75597677..75600952,3	K562	blood:
36	chr16:75593250..75596560-chr16:75613588..75617138,3	MCF-7	breast:
37	chr16:75564501..75567085-chr16:75571192..75573194,2	K562	blood:
38	chr16:75587108..75590001-chr17:56735204..56737947,2	MCF-7	breast:
39	chr16:75574262..75576234-chr16:75588612..75590836,2	MCF-7	breast:
40	chr16:75589157..75591789-chr16:75592246..75594958,4	K562	blood:
41	chr16:75583993..75586102-chr16:75587764..75590616,2	MCF-7	breast:
42	chr16:75564094..75567077-chr16:75588072..75589709,2	K562	blood:
43	chr10:97849733..97850273-chr16:75589275..75589867,2	Hela-S3	cervix:
44	chr16:75588411..75591308-chr16:75680950..75683486,5	K562	blood:
45	chr16:75574159..75575888-chr16:75581471..75583351,2	K562	blood:
46	chr16:75574159..75575888-chr16:75581471..75583351,2	K562	blood:
47	chr16:75549910..75552098-chr16:75575318..75577076,2	MCF-7	breast:
48	chr16:75587061..75591674-chr16:75591677..75597187,8	K562	blood:
49	chr16:75496858..75499850-chr16:75589381..75591063,2	K562	blood:
50	chr16:75588035..75589877-chr16:75656645..75658476,2	K562	blood:

No data

Variant related genes	Relation type
CHST5	TF binding region
TMEM231	TF binding region
ENSG00000260092	TF binding region
CHST5	CpG island
TMEM231	CpG island
ENSG00000260092	CpG island
ENSG00000034713	chromatin interactions
ENSG00000123130	chromatin interactions
ENSG00000153774	chromatin interactions
ENSG00000126458	chromatin interactions
ENSG00000164587	chromatin interactions
ENSG00000135702	chromatin interactions
ENSG00000093183	chromatin interactions
ENSG00000241839	chromatin interactions
ENSG00000114857	chromatin interactions
ENSG00000166822	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000172262	chromatin interactions
ENSG00000251445	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000153140	chromatin interactions
ENSG00000065427	chromatin interactions
ENSG00000261717	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000103111	chromatin interactions
ENSG00000226688	chromatin interactions
ENSG00000166848	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000262583	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000249240	chromatin interactions
ENSG00000205084	chromatin interactions
ENSG00000150712	chromatin interactions
ENSG00000065457	chromatin interactions

Extended variants
information (count: 1202 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3784934	chr16:75569739-75569740	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183370915	chr16:75569753-75569754	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186680929	chr16:75569765-75569766	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs557272367	chr16:75569769-75569770	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs115830852	chr16:75569771-75569772	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs547727455	chr16:75569772-75569773	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376873702	chr16:75569775-75569776	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs2641803	chr16:75569804-75569805	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535878314	chr16:75569805-75569806	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs2550884	chr16:75569815-75569816	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs544735223	chr16:75569829-75569830	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs192038599	chr16:75569853-75569854	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373074677	chr16:75569879-75569880	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs550944988	chr16:75569980-75569981	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567956643	chr16:75569992-75569993	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs377370411	chr16:75569998-75569999	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560262853	chr16:75570151-75570152	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs2550885	chr16:75570162-75570163	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs183850046	chr16:75570197-75570198	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs566899918	chr16:75570208-75570209	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs375251866	chr16:75570276-75570277	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs539121467	chr16:75570282-75570283	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs559051400	chr16:75570339-75570340	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs571352760	chr16:75570346-75570347	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs537255635	chr16:75570372-75570373	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs556939502	chr16:75570401-75570402	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs115286433	chr16:75570410-75570411	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs116248074	chr16:75570415-75570416	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs538050421	chr16:75570476-75570477	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs558284251	chr16:75570495-75570496	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552533793	chr16:75570507-75570508	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572545393	chr16:75570511-75570512	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs544700389	chr16:75570562-75570563	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs369211907	chr16:75570566-75570567	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs187763023	chr16:75570596-75570597	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs150695963	chr16:75570598-75570599	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs139836342	chr16:75570627-75570628	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs372983585	chr16:75570639-75570640	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs375584782	chr16:75570648-75570649	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs544807180	chr16:75570654-75570655	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs561396648	chr16:75570667-75570668	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs368976427	chr16:75570681-75570682	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs577824176	chr16:75570716-75570717	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs377397624	chr16:75570730-75570731	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs189556890	chr16:75570745-75570746	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566865072	chr16:75570748-75570749	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs370677083	chr16:75570789-75570790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs552344814	chr16:75570811-75570812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs149838102	chr16:75570818-75570819	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536815933	chr16:75570829-75570830	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:966 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75551200-75589200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr16:75551400-75572200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr16:75551400-75584000	Weak transcription	Right Atrium	heart
4	chr16:75551600-75575800	Weak transcription	Brain Hippocampus Middle	brain
5	chr16:75551800-75572400	Weak transcription	Right Ventricle	heart
6	chr16:75551800-75578000	Weak transcription	Fetal Brain Female	brain
7	chr16:75557800-75572400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr16:75558600-75572000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr16:75561400-75578000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr16:75561800-75579400	Weak transcription	Gastric	stomach
11	chr16:75563200-75575200	Weak transcription	Brain Angular Gyrus	brain
12	chr16:75564000-75573800	Weak transcription	Ovary	ovary
13	chr16:75564000-75578000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr16:75564200-75572400	Weak transcription	Brain Germinal Matrix	brain
15	chr16:75564200-75572600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr16:75564200-75589200	Weak transcription	Lung	lung
17	chr16:75564800-75575200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr16:75567000-75572400	Weak transcription	Brain Anterior Caudate	brain
19	chr16:75567200-75570400	Active TSS	Duodenum Mucosa	Duodenum
20	chr16:75567400-75570200	Active TSS	Rectal Mucosa Donor 31	rectum
21	chr16:75567600-75570200	Active TSS	Rectal Mucosa Donor 29	rectum
22	chr16:75568400-75570000	Active TSS	Rectal Smooth Muscle	rectum
23	chr16:75568800-75570000	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr16:75568800-75570600	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr16:75569000-75570000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr16:75569000-75570000	Active TSS	Small Intestine	intestine
27	chr16:75569000-75583800	Weak transcription	GM12878-XiMat	blood
28	chr16:75569200-75570000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr16:75569200-75570400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr16:75569200-75588600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr16:75569400-75569800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr16:75569400-75570000	Flanking Active TSS	Colonic Mucosa	Colon
33	chr16:75569400-75570000	Flanking Active TSS	Fetal Intestine Small	intestine
34	chr16:75569400-75570400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr16:75569400-75584000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr16:75569400-75588400	Weak transcription	Osteobl	bone
37	chr16:75569600-75569800	Flanking Active TSS	Fetal Intestine Large	intestine
38	chr16:75569600-75570000	Bivalent Enhancer	Fetal Stomach	stomach
39	chr16:75569600-75570000	Active TSS	Stomach Mucosa	stomach
40	chr16:75569600-75570400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr16:75569600-75578000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr16:75569800-75570000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr16:75569800-75570000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr16:75569800-75570800	Enhancers	Fetal Intestine Large	intestine
45	chr16:75570000-75570200	Enhancers	Colonic Mucosa	Colon
46	chr16:75570000-75570400	Enhancers	Stomach Mucosa	stomach
47	chr16:75570000-75570600	Enhancers	Fetal Intestine Small	intestine
48	chr16:75570000-75573800	Weak transcription	Fetal Stomach	stomach
49	chr16:75570000-75574000	Weak transcription	Small Intestine	intestine
50	chr16:75570000-75578200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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