Variant report

Variant	nsv888769
Chromosome Location	chr7:99018584-99041748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:741)
CpG islands
(count:1221)
Chromatin interactive
region (count:73)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99036361-99036588	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99036323-99036603	K562	blood:	n/a	n/a
3	ATF2	chr7:99036179-99036693	GM12878	blood:	n/a	n/a
4	ATF3	chr7:99036221-99036615	K562	blood:	n/a	chr7:99036543-99036552
5	ATF3	chr7:99036201-99036592	A549	lung:	n/a	chr7:99036543-99036552
6	BACH1	chr7:99020009-99020158	K562	blood:	n/a	n/a
7	BACH1	chr7:99036209-99036442	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr7:99036114-99036540	GM12878	blood:	n/a	n/a
9	BCLAF1	chr7:99036199-99036632	GM12878	blood:	n/a	n/a
10	BCLAF1	chr7:99036145-99036711	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:99036275-99036575	HepG2	liver:	n/a	n/a
12	BHLHE40	chr7:99036254-99036651	HepG2	liver:	n/a	chr7:99036625-99036641
13	BHLHE40	chr7:99035407-99035607	K562	blood:	n/a	n/a
14	BHLHE40	chr7:99036188-99037115	K562	blood:	n/a	chr7:99036625-99036641
15	BHLHE40	chr7:99036233-99036727	GM12878	blood:	n/a	chr7:99036625-99036641
16	BHLHE40	chr7:99019871-99020039	K562	blood:	n/a	n/a
17	BRCA1	chr7:99036472-99036534	HepG2	liver:	n/a	n/a
18	BRCA1	chr7:99036088-99036617	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr7:99036135-99036623	K562	blood:	n/a	n/a
20	CBX3	chr7:99036185-99036603	K562	blood:	n/a	n/a
21	CCNT2	chr7:99036219-99036939	K562	blood:	n/a	n/a
22	CEBPB	chr7:99036333-99036661	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:99037849-99038208	A549	lung:	n/a	chr7:99038027-99038038
24	CEBPB	chr7:99037841-99038231	A549	lung:	n/a	chr7:99038027-99038038
25	CEBPB	chr7:99037886-99038136	HepG2	liver:	n/a	chr7:99038027-99038038
26	CEBPB	chr7:99037902-99038195	Hela-S3	cervix:	n/a	chr7:99038027-99038038
27	CEBPB	chr7:99037830-99038186	K562	blood:	n/a	chr7:99038027-99038038
28	CEBPB	chr7:99037792-99038280	MCF-7	breast:	n/a	chr7:99038027-99038038
29	CEBPB	chr7:99037877-99038213	H1-hESC	embryonic stem cell:	n/a	chr7:99038027-99038038
30	CEBPB	chr7:99037853-99038245	IMR90	lung:	n/a	chr7:99038027-99038038
31	CEBPB	chr7:99037844-99038218	K562	blood:	n/a	chr7:99038027-99038038
32	CEBPB	chr7:99037822-99038190	A549	lung:	n/a	chr7:99038027-99038038
33	CEBPB	chr7:99037847-99038223	HepG2	liver:	n/a	chr7:99038027-99038038
34	CEBPB	chr7:99037850-99038231	HepG2	liver:	n/a	chr7:99038027-99038038
35	CEBPD	chr7:99036345-99036756	HepG2	liver:	n/a	n/a
36	CEBPD	chr7:99036218-99036755	HepG2	liver:	n/a	n/a
37	CHD1	chr7:99036217-99036761	GM12878	blood:	n/a	n/a
38	CHD2	chr7:99036305-99036927	GM12878	blood:	n/a	n/a
39	CHD2	chr7:99036307-99036623	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr7:99036363-99036517	HepG2	liver:	n/a	n/a
41	CHD2	chr7:99036128-99036934	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr7:99036257-99036442	K562	blood:	n/a	n/a
43	CREB1	chr7:99036095-99036855	A549	lung:	n/a	n/a
44	CREB1	chr7:99036198-99036690	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr7:99036011-99037118	GM12878	blood:	n/a	n/a
46	CREB1	chr7:99036086-99037211	HepG2	liver:	n/a	n/a
47	CREB1	chr7:99036099-99036767	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr7:99036131-99036940	K562	blood:	n/a	n/a
49	CREB1	chr7:99036306-99036632	A549	lung:	n/a	n/a
50	CTCF	chr7:99036720-99036870	AoAF	blood vessel:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99036504-99036554	Caco-2	colon:	n/a
2	chr7:99036504-99036554	Caco-2	colon:	n/a
3	chr7:99032528-99032578	AG09309	skin:	n/a
4	chr7:99034370-99034420	CMK	blood:	n/a
5	chr7:99036699-99036749	PANC-1	pancreas:	n/a
6	chr7:99036328-99036378	A549	lung:	n/a
7	chr7:99036534-99036584	HUVEC	blood vessel:	n/a
8	chr7:99034370-99034420	HepG2	liver:	n/a
9	chr7:99040005-99040055	HCT-116	colon:	n/a
10	chr7:99036512-99036562	HCF	heart:	n/a
11	chr7:99036343-99036393	K562	blood:	n/a
12	chr7:99034370-99034420	Hela-S3	cervix:	n/a
13	chr7:99037189-99037239	AG04450	lung:	fetal
14	chr7:99037189-99037239	MCF10A-Er-Src	breast:	n/a
15	chr7:99036756-99036806	HCT-116	colon:	n/a
16	chr7:99036699-99036749	HCM	heart:	n/a
17	chr7:99019985-99020035	HNPCEpiC	eye:	n/a
18	chr7:99036504-99036554	HUVEC	blood vessel:	n/a
19	chr7:99036504-99036554	A549	lung:	n/a
20	chr7:99040005-99040055	HCM	heart:	n/a
21	chr7:99036546-99036596	HAEpiC	amniotic membrane:	n/a
22	chr7:99036756-99036806	SK-N-SH	brain:	n/a
23	chr7:99019985-99020035	AG10803	skin:	n/a
24	chr7:99036501-99036551	HCT-116	colon:	n/a
25	chr7:99036496-99036546	HCPEpiC	choroid plexus:	n/a
26	chr7:99036702-99036752	NT2-D1	testis:	n/a
27	chr7:99036699-99036749	SK-N-SH_RA	brain:	n/a
28	chr7:99036512-99036562	BE2_C	brain:	n/a
29	chr7:99040005-99040055	LNCaP	prostate:	n/a
30	chr7:99036504-99036554	HEK293	kidney:	embryo
31	chr7:99036501-99036551	HL-60	blood:	n/a
32	chr7:99036504-99036554	GM06990	blood:	n/a
33	chr7:99036841-99036891	CMK	blood:	n/a
34	chr7:99037189-99037239	HCT-116	colon:	n/a
35	chr7:99036501-99036551	MCF10A-Er-Src	breast:	n/a
36	chr7:99036534-99036584	HCPEpiC	choroid plexus:	n/a
37	chr7:99019985-99020035	CMK	blood:	n/a
38	chr7:99032677-99032727	IMR90	lung:	fetal
39	chr7:99040005-99040055	HRE	kidney:	n/a
40	chr7:99034370-99034420	HNPCEpiC	eye:	n/a
41	chr7:99036702-99036752	HRE	kidney:	n/a
42	chr7:99036512-99036562	SK-N-SH	brain:	n/a
43	chr7:99037189-99037239	HMEC	breast:	n/a
44	chr7:99036512-99036562	NT2-D1	testis:	n/a
45	chr7:99036343-99036393	ECC-1	luminal epithelium:	n/a
46	chr7:99036841-99036891	HEK293	kidney:	embryo
47	chr7:99036702-99036752	GM12891	blood:	n/a
48	chr7:99019985-99020035	NHDF-neo	bronchial:	n/a
49	chr7:99040005-99040055	HepG2	liver:	n/a
50	chr7:99036496-99036546	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:99024108..99026469-chr7:99034518..99036829,2	MCF-7	breast:
2	chr7:99020436..99022117-chr7:99066958..99069565,2	MCF-7	breast:
3	chr7:99019797..99022684-chr7:99036471..99038097,2	MCF-7	breast:
4	chr2:239228602..239229208-chr7:99036122..99036622,2	HCT-116	colon:
5	chr7:99021211..99022744-chr7:99025529..99028020,2	MCF-7	breast:
6	chr7:99034720..99038160-chr7:99048984..99054018,5	MCF-7	breast:
7	chr7:99035477..99037165-chr7:100025272..100027414,2	K562	blood:
8	chr7:99036970..99039265-chr7:99039739..99041583,2	MCF-7	breast:
9	chr7:99004290..99006114-chr7:99025633..99027496,2	K562	blood:
10	chr6:134495044..134495795-chr7:99036121..99037024,2	Hela-S3	cervix:
11	chr7:98739484..98741856-chr7:99035435..99038061,2	K562	blood:
12	chr7:99021541..99023967-chr7:99034464..99036526,2	MCF-7	breast:
13	chr7:99003930..99008101-chr7:99034839..99037079,5	K562	blood:
14	chr7:99001484..99003635-chr7:99032738..99035703,2	K562	blood:
15	chr7:99004207..99009187-chr7:99032699..99039268,13	MCF-7	breast:
16	chr7:99030944..99035080-chr7:99035226..99039444,6	MCF-7	breast:
17	chr7:99035431..99038374-chr7:99696976..99699327,2	K562	blood:
18	chr7:99005761..99007888-chr7:99034840..99036856,3	K562	blood:
19	chr7:75544201..75544974-chr7:99036458..99037062,2	NB4	blood:
20	chr7:99035601..99038053-chr7:99042124..99044102,2	MCF-7	breast:
21	chr7:99007985..99010894-chr7:99027343..99030538,3	MCF-7	breast:
22	chr7:99004073..99007178-chr7:99034881..99037749,7	MCF-7	breast:
23	chr11:62608557..62609372-chr7:99036141..99036767,2	Hela-S3	cervix:
24	chr7:99026847..99029073-chr7:99029475..99031383,3	K562	blood:
25	chr7:99004763..99008262-chr7:99018470..99023968,5	MCF-7	breast:
26	chr7:99027922..99030424-chr7:99032965..99035110,3	K562	blood:
27	chr7:99036970..99039265-chr7:99039739..99041583,2	MCF-7	breast:
28	chr7:99007762..99009828-chr7:99020808..99022808,2	MCF-7	breast:
29	chr7:99020429..99023882-chr7:99024975..99028179,3	K562	blood:
30	chr7:99020429..99023882-chr7:99024975..99028179,3	K562	blood:
31	chr7:99034906..99037926-chr7:99095119..99098935,4	K562	blood:
32	chr7:99014925..99017023-chr7:99029378..99031176,2	K562	blood:
33	chr7:98970707..98973711-chr7:99034539..99037806,4	MCF-7	breast:
34	chr7:99038361..99041126-chr7:99102588..99104976,2	K562	blood:
35	chr7:99021211..99022744-chr7:99025529..99028020,2	MCF-7	breast:
36	chr7:98971332..98973489-chr7:99034701..99036393,2	MCF-7	breast:
37	chr4:6717498..6717998-chr7:99036106..99036609,2	Hela-S3	cervix:
38	chr7:99027922..99030424-chr7:99032965..99035110,3	K562	blood:
39	chr7:99020471..99023882-chr7:99024975..99028185,3	K562	blood:
40	chr7:99025099..99027768-chr7:99034111..99036844,3	MCF-7	breast:
41	chr7:99034517..99037333-chr7:99070217..99072293,2	K562	blood:
42	chr7:99036051..99038082-chr7:99079952..99081854,3	K562	blood:
43	chr7:99010009..99013201-chr7:99032916..99037248,5	MCF-7	breast:
44	chr7:99036383..99037983-chr7:99697616..99700262,2	MCF-7	breast:
45	chr7:99034954..99037975-chr7:99677842..99679932,3	K562	blood:
46	chr7:99004079..99005950-chr7:99029849..99032633,2	MCF-7	breast:
47	chr7:99019766..99021951-chr7:99025804..99027414,2	MCF-7	breast:
48	chr7:99028798..99032281-chr7:99034267..99038059,8	MCF-7	breast:
49	chr7:99015616..99019079-chr7:99036189..99039194,4	MCF-7	breast:
50	chr7:99034954..99037866-chr7:99677567..99679393,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000228335	TF binding region
PTCD1	TF binding region
ENSG00000214314	TF binding region
CPSF4	TF binding region
ENSG00000228335	CpG island
PTCD1	CpG island
ENSG00000214314	CpG island
CPSF4	CpG island
ENSG00000248919	chromatin interactions
ENSG00000228335	chromatin interactions
ENSG00000221838	chromatin interactions
ENSG00000160917	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000214314	chromatin interactions
ENSG00000127948	chromatin interactions
ENSG00000130429	chromatin interactions
ENSG00000204104	chromatin interactions
ENSG00000198742	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000265020	chromatin interactions
ENSG00000106246	chromatin interactions
ENSG00000196652	chromatin interactions
ENSG00000239133	chromatin interactions
ENSG00000160908	chromatin interactions
ENSG00000241468	chromatin interactions
ENSG00000166526	chromatin interactions
ENSG00000198556	chromatin interactions
ENSG00000106244	chromatin interactions
ENSG00000106245	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000118515	chromatin interactions
ENSG00000164548	chromatin interactions
ENSG00000186222	chromatin interactions

Extended variants
information (count: 1057 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1057 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9691511	chr7:99018584-99018585	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs535751183	chr7:99018636-99018637	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs141950481	chr7:99018669-99018670	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs549476059	chr7:99018680-99018681	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs141768682	chr7:99018696-99018697	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs567710012	chr7:99018700-99018701	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs192162960	chr7:99018702-99018703	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs556478561	chr7:99018711-99018712	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs554974850	chr7:99018738-99018739	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs150665020	chr7:99018743-99018744	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs572581514	chr7:99018762-99018763	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs563940335	chr7:99018792-99018793	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs139042286	chr7:99018799-99018800	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs183680021	chr7:99018840-99018841	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs573362351	chr7:99018921-99018922	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs543809715	chr7:99018924-99018925	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs9690310	chr7:99018967-99018968	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs189076228	chr7:99019019-99019020	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs533093005	chr7:99019045-99019046	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs555898363	chr7:99019053-99019054	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs551636327	chr7:99019058-99019059	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs528229166	chr7:99019064-99019065	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs56395258	chr7:99019067-99019068	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs375317840	chr7:99019071-99019072	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs201868635	chr7:99019075-99019076	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs35248579	chr7:99019077-99019078	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs374285286	chr7:99019086-99019087	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184655736	chr7:99019095-99019096	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs145949187	chr7:99019150-99019151	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs567767477	chr7:99019156-99019157	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs370543783	chr7:99019165-99019166	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs549927713	chr7:99019215-99019216	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs139819601	chr7:99019221-99019222	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs538994023	chr7:99019238-99019239	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs189495890	chr7:99019264-99019265	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs191862806	chr7:99019265-99019266	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs56992635	chr7:99019279-99019280	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs554696987	chr7:99019306-99019307	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs573425273	chr7:99019307-99019308	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs60996680	chr7:99019311-99019312	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs374687726	chr7:99019313-99019314	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs577543345	chr7:99019315-99019316	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs565377207	chr7:99019320-99019321	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs545021225	chr7:99019322-99019323	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs560385648	chr7:99019371-99019372	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs527539698	chr7:99019374-99019375	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs61283116	chr7:99019413-99019414	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs561034240	chr7:99019453-99019454	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs377395752	chr7:99019457-99019458	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs184249973	chr7:99019458-99019459	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	18632612	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1498 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99007200-99035400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:99007800-99024000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr7:99008000-99019800	Weak transcription	Right Atrium	heart
4	chr7:99008000-99023400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr7:99008000-99023600	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:99008000-99023800	Strong transcription	H1 Cell Line	embryonic stem cell
7	chr7:99008000-99023800	Strong transcription	Placenta	Placenta
8	chr7:99008000-99024000	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:99008000-99024000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:99008000-99024000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr7:99008000-99024000	Strong transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:99008000-99024000	Strong transcription	Spleen	Spleen
13	chr7:99008000-99024200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr7:99008000-99024200	Strong transcription	Fetal Stomach	stomach
15	chr7:99008000-99026600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr7:99008200-99023400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
17	chr7:99008200-99023600	Strong transcription	Fetal Intestine Large	intestine
18	chr7:99008200-99023800	Strong transcription	Cortex derived primary cultured neurospheres	brain
19	chr7:99008200-99023800	Strong transcription	Fetal Brain Female	brain
20	chr7:99008200-99023800	Strong transcription	Fetal Muscle Trunk	muscle
21	chr7:99008200-99023800	Strong transcription	Fetal Muscle Leg	muscle
22	chr7:99008200-99024000	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr7:99008200-99024000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr7:99008200-99024000	Strong transcription	Lung	lung
25	chr7:99008200-99024200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr7:99008400-99018800	Strong transcription	Fetal Lung	lung
27	chr7:99008400-99018800	Strong transcription	Rectal Mucosa Donor 31	rectum
28	chr7:99008400-99019000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:99008400-99019000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr7:99008400-99019000	Strong transcription	Stomach Smooth Muscle	stomach
31	chr7:99008400-99019200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr7:99008400-99019400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr7:99008400-99023200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:99008400-99023400	Strong transcription	Fetal Thymus	thymus
35	chr7:99008400-99023600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:99008400-99023600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr7:99008400-99023600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:99008400-99023600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr7:99008400-99023800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:99008400-99023800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:99008400-99024000	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr7:99008600-99018600	Strong transcription	HMEC	breast
43	chr7:99008600-99018800	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr7:99008600-99019000	Strong transcription	Primary B cells from peripheral blood	blood
45	chr7:99008600-99023000	Strong transcription	Osteobl	bone
46	chr7:99008600-99023200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:99008600-99023200	Strong transcription	Duodenum Mucosa	Duodenum
48	chr7:99008600-99023200	Strong transcription	NHEK	skin
49	chr7:99008600-99023600	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr7:99008600-99023600	Strong transcription	Primary T cells from cord blood	blood

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