Variant report

Variant	nsv530715
Chromosome Location	chr16:81117168-81252875
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2355)
CpG islands
(count:1283)
Chromatin interactive
region (count:173)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2355 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:81248492-81248727	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:81130145-81130435	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:81156626-81157063	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:81208937-81209198	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:81214625-81215127	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:81238678-81239059	K562	blood:	n/a	n/a
7	ARID3A	chr16:81127466-81127520	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:81214892-81214996	K562	blood:	n/a	n/a
9	ARID3A	chr16:81224425-81224545	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:81232328-81232582	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:81238745-81239052	HepG2	liver:	n/a	n/a
12	ATF1	chr16:81131370-81131588	K562	blood:	n/a	n/a
13	ATF1	chr16:81223002-81223299	K562	blood:	n/a	n/a
14	ATF1	chr16:81156756-81157044	K562	blood:	n/a	n/a
15	ATF1	chr16:81130024-81130677	K562	blood:	n/a	n/a
16	ATF1	chr16:81214812-81215125	K562	blood:	n/a	n/a
17	ATF3	chr16:81214756-81215189	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr16:81214868-81215234	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr16:81222914-81223172	K562	blood:	n/a	n/a
20	ATF3	chr16:81214880-81215235	K562	blood:	n/a	n/a
21	ATF3	chr16:81214923-81215132	K562	blood:	n/a	n/a
22	ATF3	chr16:81208842-81209330	A549	lung:	n/a	n/a
23	BACH1	chr16:81174746-81175382	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr16:81175001-81175341	K562	blood:	n/a	n/a
25	BACH1	chr16:81189210-81189228	K562	blood:	n/a	n/a
26	BATF	chr16:81168205-81168486	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:81168284-81168501	GM12878	blood:	n/a	n/a
28	BCL3	chr16:81199974-81200763	GM12878	blood:	n/a	n/a
29	BCL3	chr16:81206697-81207272	GM12878	blood:	n/a	chr16:81207055-81207064 chr16:81207056-81207065
30	BCL3	chr16:81206605-81207349	GM12878	blood:	n/a	chr16:81207055-81207064 chr16:81207056-81207065
31	BCL3	chr16:81143404-81143722	GM12878	blood:	n/a	n/a
32	BCL3	chr16:81199969-81200597	GM12878	blood:	n/a	n/a
33	BHLHE40	chr16:81163135-81163164	K562	blood:	n/a	n/a
34	BHLHE40	chr16:81204595-81204730	K562	blood:	n/a	n/a
35	BHLHE40	chr16:81204462-81204796	HepG2	liver:	n/a	n/a
36	BHLHE40	chr16:81129357-81130537	K562	blood:	n/a	n/a
37	BHLHE40	chr16:81170170-81170518	HepG2	liver:	n/a	chr16:81170312-81170321
38	BHLHE40	chr16:81129544-81129723	GM12878	blood:	n/a	n/a
39	BHLHE40	chr16:81248487-81248577	K562	blood:	n/a	n/a
40	BHLHE40	chr16:81204484-81204816	HepG2	liver:	n/a	n/a
41	BHLHE40	chr16:81154295-81154311	HepG2	liver:	n/a	n/a
42	BHLHE40	chr16:81238713-81238961	K562	blood:	n/a	n/a
43	BHLHE40	chr16:81222771-81223296	K562	blood:	n/a	n/a
44	BHLHE40	chr16:81200163-81200265	K562	blood:	n/a	n/a
45	BHLHE40	chr16:81170261-81170322	K562	blood:	n/a	chr16:81170312-81170321
46	BHLHE40	chr16:81224490-81224559	K562	blood:	n/a	n/a
47	BHLHE40	chr16:81129468-81129903	HepG2	liver:	n/a	n/a
48	BHLHE40	chr16:81214654-81214874	K562	blood:	n/a	n/a
49	BRCA1	chr16:81200424-81200502	GM12878	blood:	n/a	n/a
50	BRCA1	chr16:81232353-81232533	HepG2	liver:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81130375-81130425	PANC-1	pancreas:	n/a
2	chr16:81130217-81130267	Jurkat	blood:	n/a
3	chr16:81130375-81130425	PANC-1	pancreas:	n/a
4	chr16:81130217-81130267	Jurkat	blood:	n/a
5	chr16:81248670-81248720	Jurkat	blood:	n/a
6	chr16:81129318-81129368	HEK293	kidney:	embryo
7	chr16:81248670-81248720	SKMC	muscle:	n/a
8	chr16:81248670-81248720	SK-N-MC	brain:	n/a
9	chr16:81134712-81134762	U87	brain:	n/a
10	chr16:81129997-81130047	SK-N-MC	brain:	n/a
11	chr16:81130375-81130425	NT2-D1	testis:	n/a
12	chr16:81132798-81132848	ProgFib	skin:	n/a
13	chr16:81190494-81190544	HEK293	kidney:	embryo
14	chr16:81170527-81170577	HCT-116	colon:	n/a
15	chr16:81132798-81132848	RPTEC	kidney:	n/a
16	chr16:81130092-81130142	ProgFib	skin:	n/a
17	chr16:81130375-81130425	SK-N-MC	brain:	n/a
18	chr16:81130092-81130142	U87	brain:	n/a
19	chr16:81208471-81208521	A549	lung:	n/a
20	chr16:81129997-81130047	Hela-S3	cervix:	n/a
21	chr16:81248670-81248720	MCF10A-Er-Src	breast:	n/a
22	chr16:81190494-81190544	HCPEpiC	choroid plexus:	n/a
23	chr16:81129991-81130041	PFSK-1	brain:	n/a
24	chr16:81190547-81190597	ECC-1	luminal epithelium:	n/a
25	chr16:81130092-81130142	HAEpiC	amniotic membrane:	n/a
26	chr16:81223254-81223304	HCPEpiC	choroid plexus:	n/a
27	chr16:81190547-81190597	IMR90	lung:	fetal
28	chr16:81130346-81130396	U87	brain:	n/a
29	chr16:81129369-81129419	NT2-D1	testis:	n/a
30	chr16:81134712-81134762	Jurkat	blood:	n/a
31	chr16:81130092-81130142	HMEC	breast:	n/a
32	chr16:81132798-81132848	MCF10A-Er-Src	breast:	n/a
33	chr16:81248670-81248720	HUVEC	blood vessel:	n/a
34	chr16:81190547-81190597	NHDF-neo	bronchial:	n/a
35	chr16:81130217-81130267	HRCEpiC	kidney:	n/a
36	chr16:81130120-81130170	SK-N-SH	brain:	n/a
37	chr16:81130346-81130396	PANC-1	pancreas:	n/a
38	chr16:81129369-81129419	AG10803	skin:	n/a
39	chr16:81208471-81208521	IMR90	lung:	fetal
40	chr16:81129997-81130047	HNPCEpiC	eye:	n/a
41	chr16:81132798-81132848	A549	lung:	n/a
42	chr16:81190494-81190544	NHBE	bronchial:	n/a
43	chr16:81132798-81132848	HEEpiC	esophagus:	n/a
44	chr16:81129997-81130047	MCF-7	breast:	n/a
45	chr16:81129997-81130047	GM19239	blood:	n/a
46	chr16:81208471-81208521	SK-N-MC	brain:	n/a
47	chr16:81130120-81130170	HAEpiC	amniotic membrane:	n/a
48	chr16:81130346-81130396	AG10803	skin:	n/a
49	chr16:81208471-81208521	AoSMC	blood vessel:	n/a
50	chr16:81170527-81170577	HIPEpiC	eye:	n/a

(count:173 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr16:81232049..81234951-chr16:81236497..81238711,3	MCF-7	breast:
2	chr16:81207703..81209401-chr16:81309474..81311615,2	MCF-7	breast:
3	chr16:81241192..81243910-chr16:81245039..81247038,2	K562	blood:
4	chr16:81109242..81112738-chr16:81125910..81131139,12	MCF-7	breast:
5	chr16:81237375..81239298-chr16:81246693..81248653,2	K562	blood:
6	chr16:81238393..81239236-chr16:81383637..81384525,3	MCF-7	breast:
7	chr16:81152674..81158113-chr16:81158859..81162763,5	K562	blood:
8	chr11:62480881..62483746-chr16:81123600..81125126,2	MCF-7	breast:
9	chr16:81248661..81251389-chr16:81251410..81253409,3	K562	blood:
10	chr16:81160894..81162615-chr16:81168602..81170831,2	MCF-7	breast:
11	chr16:81203969..81206813-chr16:81207066..81208613,2	MCF-7	breast:
12	chr1:152741230..152741815-chr16:81212739..81213485,2	MCF-7	breast:
13	chr16:81108969..81114076-chr16:81128464..81132360,7	K562	blood:
14	chr16:81128667..81130773-chr16:81131741..81134300,2	MCF-7	breast:
15	chr16:81104177..81106310-chr16:81122487..81125294,2	K562	blood:
16	chr16:81167266..81170181-chr16:81212814..81215037,2	MCF-7	breast:
17	chr16:81130019..81131773-chr16:81135530..81138449,2	K562	blood:
18	chr16:81038549..81041288-chr16:81132272..81134498,2	K562	blood:
19	chr16:81068494..81071039-chr16:81229020..81231792,3	MCF-7	breast:
20	chr16:81069222..81069838-chr16:81238638..81239329,2	MCF-7	breast:
21	chr16:81068953..81069797-chr16:81176232..81177093,2	K562	blood:
22	chr16:81212604..81215452-chr16:81226306..81228554,2	MCF-7	breast:
23	chr16:81116747..81118686-chr16:81121475..81123225,2	K562	blood:
24	chr16:81109459..81113813-chr16:81119137..81125158,9	MCF-7	breast:
25	chr16:81123255..81125056-chr16:81127455..81129707,2	MCF-7	breast:
26	chr16:81172576..81173403-chr16:81248138..81248840,3	MCF-7	breast:
27	chr16:81176050..81179014-chr16:81206703..81209353,3	MCF-7	breast:
28	chr16:81191490..81193382-chr16:81194384..81196208,2	MCF-7	breast:
29	chr16:81115837..81117443-chr16:81124518..81126684,3	K562	blood:
30	chr16:81129494..81132038-chr16:81235972..81238926,2	MCF-7	breast:
31	chr16:81078751..81080848-chr16:81181095..81182686,2	K562	blood:
32	chr16:81039111..81042091-chr16:81131038..81132906,2	MCF-7	breast:
33	chr16:81170203..81172478-chr16:81173151..81175133,2	MCF-7	breast:
34	chr16:81069305..81071127-chr16:81245572..81248364,2	MCF-7	breast:
35	chr16:81144641..81147078-chr16:81149251..81151936,2	K562	blood:
36	chr16:81194645..81197115-chr16:81199955..81201800,2	MCF-7	breast:
37	chr16:81187277..81187855-chr16:81231986..81232826,2	MCF-7	breast:
38	chr16:81068894..81069816-chr16:81231960..81232923,14	MCF-7	breast:
39	chr16:81068395..81070706-chr16:81144379..81146782,2	K562	blood:
40	chr12:108895394..108895894-chr16:81238428..81239017,2	MCF-7	breast:
41	chr16:81109532..81111432-chr16:81117423..81118984,2	MCF-7	breast:
42	chr16:81238408..81239122-chr16:81294572..81295294,2	K562	blood:
43	chr16:81128142..81131437-chr16:81131479..81134618,4	K562	blood:
44	chr16:81068964..81069731-chr16:81231614..81232947,4	MCF-7	breast:
45	chr16:81177157..81179228-chr16:81223964..81225695,2	MCF-7	breast:
46	chr16:81181423..81183511-chr16:81191451..81193447,2	MCF-7	breast:
47	chr16:81129115..81131910-chr16:81152675..81155542,2	K562	blood:
48	chr16:81152674..81158113-chr16:81158859..81162763,5	K562	blood:
49	chr16:81242972..81244924-chr16:81246844..81249498,3	MCF-7	breast:
50	chr16:81202808..81207445-chr16:81207542..81212680,8	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GCSH-2	chr16:81165896-81166137	l_1369_chr16:81136436-81166565_testes
2	lnc-GCSH-2	chr16:81166255-81166565	l_1369_chr16:81136436-81166565_testes
3	lnc-GCSH-2	chr16:81136437-81136565	l_1369_chr16:81136436-81166565_testes
4	lnc-GCSH-2	chr16:81145264-81145354	l_1369_chr16:81136436-81166565_testes

No data

Variant related genes	Relation type
ENSG00000260643	TF binding region
RNU6-1191P	TF binding region
GCSH	TF binding region
PKD1L2	TF binding region
ENSG00000260643	CpG island
RNU6-1191P	CpG island
GCSH	CpG island
PKD1L2	CpG island
ENSG00000156508	chromatin interactions
ENSG00000261061	chromatin interactions
ENSG00000260643	chromatin interactions
ENSG00000245059	chromatin interactions
ENSG00000166455	chromatin interactions
ENSG00000261838	chromatin interactions
ENSG00000252608	chromatin interactions
ENSG00000166451	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000140905	chromatin interactions
ENSG00000260228	chromatin interactions
ENSG00000103121	chromatin interactions
ENSG00000261218	chromatin interactions
ENSG00000261609	chromatin interactions
ENSG00000166747	chromatin interactions
ENSG00000166473	chromatin interactions
ENSG00000260213	chromatin interactions

Extended variants
information (count: 9348 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:9348 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186243201	chr16:81117192-81117193	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs564865446	chr16:81117195-81117196	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs538476374	chr16:81117217-81117218	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556432931	chr16:81117234-81117235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200390845	chr16:81117261-81117262	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564804532	chr16:81117263-81117264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs8177941	chr16:81117269-81117270	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs539306849	chr16:81117354-81117355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs8177940	chr16:81117394-81117395	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs572102715	chr16:81117402-81117403	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542632695	chr16:81117432-81117433	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs368413654	chr16:81117453-81117454	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113787805	chr16:81117461-81117462	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs76656387	chr16:81117467-81117468	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
15	rs16954599	chr16:81117504-81117505	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543608292	chr16:81117512-81117513	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs549561758	chr16:81117518-81117519	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs4888119	chr16:81117546-81117547	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs191093063	chr16:81117583-81117584	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs145422690	chr16:81117588-81117589	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs79832284	chr16:81117589-81117590	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs569740769	chr16:81117600-81117601	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs147698403	chr16:81117640-81117641	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs527718224	chr16:81117659-81117660	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs142320976	chr16:81117688-81117689	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375184214	chr16:81117728-81117729	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs567750194	chr16:81117770-81117771	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs531669814	chr16:81117772-81117773	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs550367750	chr16:81117781-81117782	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs59034169	chr16:81117789-81117790	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs397963792	chr16:81117792-81117793	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571843179	chr16:81117796-81117797	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539217189	chr16:81117801-81117802	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs56395947	chr16:81117806-81117807	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs56286107	chr16:81117832-81117833	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs536299301	chr16:81117847-81117848	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554544781	chr16:81117865-81117866	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143239582	chr16:81117875-81117876	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs576097010	chr16:81117897-81117898	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs56032321	chr16:81117906-81117907	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs558598354	chr16:81117955-81117956	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs200064276	chr16:81117976-81117977	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs199824842	chr16:81118020-81118021	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs373604943	chr16:81118039-81118040	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576661048	chr16:81118044-81118045	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs112187220	chr16:81118046-81118047	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs377580970	chr16:81118056-81118057	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs540817676	chr16:81118079-81118080	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs559267379	chr16:81118098-81118099	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs140749911	chr16:81118154-81118155	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81111400-81117200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr16:81111400-81122400	Weak transcription	Lung	lung
3	chr16:81111400-81122600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr16:81111400-81122800	Weak transcription	Ovary	ovary
5	chr16:81111400-81128200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr16:81111400-81128400	Weak transcription	Aorta	Aorta
7	chr16:81111400-81128800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr16:81111400-81128800	Weak transcription	Psoas Muscle	Psoas
9	chr16:81111400-81128800	Weak transcription	NHDF-Ad	bronchial
10	chr16:81111400-81129000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr16:81111400-81129000	Weak transcription	Gastric	stomach
12	chr16:81111400-81129200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr16:81111600-81117200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr16:81111600-81117400	Weak transcription	Spleen	Spleen
15	chr16:81111600-81117600	Weak transcription	Fetal Intestine Small	intestine
16	chr16:81111600-81119200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr16:81111600-81120200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr16:81111600-81120800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr16:81111600-81122000	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr16:81111600-81122200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr16:81111600-81122400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr16:81111600-81122400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr16:81111600-81122400	Weak transcription	Fetal Intestine Large	intestine
24	chr16:81111600-81122400	Weak transcription	NHEK	skin
25	chr16:81111600-81122800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr16:81111600-81122800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr16:81111600-81123000	Weak transcription	Primary T cells from cord blood	blood
28	chr16:81111600-81123000	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr16:81111600-81123000	Weak transcription	HMEC	breast
30	chr16:81111600-81123200	Weak transcription	Duodenum Mucosa	Duodenum
31	chr16:81111600-81123200	Weak transcription	Placenta	Placenta
32	chr16:81111600-81125600	Weak transcription	GM12878-XiMat	blood
33	chr16:81111600-81127800	Weak transcription	Brain Substantia Nigra	brain
34	chr16:81111600-81128000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr16:81111600-81128200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr16:81111600-81128200	Weak transcription	Brain Hippocampus Middle	brain
37	chr16:81111600-81128200	Weak transcription	NH-A	brain
38	chr16:81111600-81128400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr16:81111600-81128400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr16:81111600-81128400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr16:81111600-81128400	Weak transcription	Brain Anterior Caudate	brain
42	chr16:81111600-81128400	Weak transcription	Fetal Muscle Trunk	muscle
43	chr16:81111600-81128400	Weak transcription	HSMM	muscle
44	chr16:81111600-81128600	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr16:81111600-81128600	Weak transcription	Fetal Kidney	kidney
46	chr16:81111600-81128600	Weak transcription	Pancreas	Pancrea
47	chr16:81111600-81128800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr16:81111600-81128800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr16:81111600-81128800	Weak transcription	Primary B cells from peripheral blood	blood
50	chr16:81111600-81128800	Weak transcription	Primary T cells fromperipheralblood	blood

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