Variant report

Variant	nsv1000199
Chromosome Location	chr1:223803545-223854859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:223803986-223804103	K562	blood:	n/a	n/a
2	ATF3	chr1:223816000-223816218	K562	blood:	n/a	n/a
3	BACH1	chr1:223834947-223834971	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:223819895-223820243	GM12878	blood:	n/a	n/a
5	BATF	chr1:223809028-223809426	GM12878	blood:	n/a	n/a
6	BATF	chr1:223809024-223809509	GM12878	blood:	n/a	n/a
7	BATF	chr1:223808049-223808372	GM12878	blood:	n/a	chr1:223808205-223808216
8	BCL11A	chr1:223809058-223809350	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:223808999-223809391	GM12878	blood:	n/a	n/a
10	BCL3	chr1:223809039-223809430	GM12878	blood:	n/a	n/a
11	BCL3	chr1:223842759-223843334	A549	lung:	n/a	n/a
12	BHLHE40	chr1:223809040-223809519	GM12878	blood:	n/a	n/a
13	BHLHE40	chr1:223815889-223816261	K562	blood:	n/a	n/a
14	CBX3	chr1:223815860-223816359	K562	blood:	n/a	n/a
15	CEBPB	chr1:223826953-223827268	K562	blood:	n/a	chr1:223827097-223827108
16	CEBPB	chr1:223851813-223852188	HepG2	liver:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
17	CEBPB	chr1:223851805-223852209	A549	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
18	CEBPB	chr1:223851815-223852192	K562	blood:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
19	CEBPB	chr1:223822220-223822370	HepG2	liver:	n/a	n/a
20	CEBPB	chr1:223851823-223852172	IMR90	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
21	CEBPB	chr1:223826932-223827280	Hela-S3	cervix:	n/a	chr1:223827097-223827108
22	CEBPB	chr1:223851859-223852168	H1-hESC	embryonic stem cell:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
23	CEBPB	chr1:223826966-223827207	HepG2	liver:	n/a	chr1:223827097-223827108
24	CEBPB	chr1:223826960-223827254	A549	lung:	n/a	chr1:223827097-223827108
25	CEBPB	chr1:223826873-223827448	MCF-7	breast:	n/a	chr1:223827097-223827108
26	CEBPB	chr1:223851818-223852190	A549	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
27	CEBPB	chr1:223851839-223852173	Hela-S3	cervix:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
28	CEBPB	chr1:223851866-223852042	HepG2	liver:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
29	CEBPB	chr1:223840146-223840530	MCF-7	breast:	n/a	n/a
30	CEBPB	chr1:223812732-223812865	K562	blood:	n/a	n/a
31	CEBPB	chr1:223851716-223852214	MCF-7	breast:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
32	CEBPB	chr1:223826848-223827494	MCF-7	breast:	n/a	chr1:223827097-223827108
33	CEBPB	chr1:223851821-223852161	K562	blood:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
34	CEBPB	chr1:223851845-223852146	ECC-1	luminal epithelium:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
35	CEBPB	chr1:223851734-223852179	MCF-7	breast:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
36	CEBPB	chr1:223826952-223827252	K562	blood:	n/a	chr1:223827097-223827108
37	CEBPB	chr1:223842598-223843268	MCF-7	breast:	n/a	n/a
38	CEBPB	chr1:223844841-223844933	HepG2	liver:	n/a	chr1:223844867-223844880 chr1:223844866-223844883 chr1:223844867-223844880
39	CEBPB	chr1:223851676-223852259	A549	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
40	CEBPB	chr1:223835053-223835253	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:223825571-223825761	IMR90	lung:	n/a	n/a
42	CHD2	chr1:223809987-223810219	HepG2	liver:	n/a	n/a
43	CREB1	chr1:223841773-223842325	A549	lung:	n/a	n/a
44	CREB1	chr1:223809010-223809535	GM12878	blood:	n/a	n/a
45	CTCF	chr1:223816020-223816170	HPF	lung:	n/a	chr1:223816071-223816078 chr1:223816066-223816079 chr1:223816065-223816081 chr1:223816066-223816079 chr1:223816059-223816080 chr1:223816064-223816082
46	CTCF	chr1:223816000-223816150	GM12871	blood:	n/a	chr1:223816071-223816078 chr1:223816066-223816079 chr1:223816065-223816081 chr1:223816066-223816079 chr1:223816059-223816080 chr1:223816064-223816082
47	CTCF	chr1:223819120-223819270	HMEC	breast:	n/a	n/a
48	CTCF	chr1:223815980-223816130	HPAF	blood vessel:	n/a	chr1:223816071-223816078 chr1:223816066-223816079 chr1:223816065-223816081 chr1:223816066-223816079 chr1:223816059-223816080 chr1:223816064-223816082
49	CTCF	chr1:223805145-223805259	LNCaP	prostate:	n/a	n/a
50	CTCF	chr1:223809208-223809503	GM12878	blood:	n/a	chr1:223809448-223809457

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223835369-223835419	HL-60	blood:	n/a
2	chr1:223835369-223835419	HL-60	blood:	n/a
3	chr1:223853145-223853195	GM06990	blood:	n/a
4	chr1:223853949-223853999	NHDF-neo	bronchial:	n/a
5	chr1:223840974-223841024	MCF-7	breast:	n/a
6	chr1:223853145-223853195	U87	brain:	n/a
7	chr1:223840925-223840975	GM12878	blood:	n/a
8	chr1:223854639-223854689	H1-hESC	embryonic stem cell:	embryo
9	chr1:223840974-223841024	HCM	heart:	n/a
10	chr1:223853949-223853999	HL-60	blood:	n/a
11	chr1:223854704-223854754	Hepatocyte	liver:	n/a
12	chr1:223854447-223854497	NH-A	brain:	n/a
13	chr1:223853928-223853978	HCM	heart:	n/a
14	chr1:223835369-223835419	HIPEpiC	eye:	n/a
15	chr1:223854704-223854754	AG09319	gingival:	n/a
16	chr1:223854447-223854497	NHDF-neo	bronchial:	n/a
17	chr1:223840925-223840975	CMK	blood:	n/a
18	chr1:223853928-223853978	AG04450	lung:	fetal
19	chr1:223853928-223853978	HMEC	breast:	n/a
20	chr1:223835369-223835419	NT2-D1	testis:	n/a
21	chr1:223854447-223854497	SAEC	small airway:	n/a
22	chr1:223853928-223853978	GM19239	blood:	n/a
23	chr1:223840974-223841024	SK-N-MC	brain:	n/a
24	chr1:223854447-223854497	Jurkat	blood:	n/a
25	chr1:223840925-223840975	MCF-7	breast:	n/a
26	chr1:223853145-223853195	SK-N-SH	brain:	n/a
27	chr1:223854639-223854689	HL-60	blood:	n/a
28	chr1:223854704-223854754	ECC-1	luminal epithelium:	n/a
29	chr1:223840974-223841024	SAEC	small airway:	n/a
30	chr1:223854704-223854754	SAEC	small airway:	n/a
31	chr1:223835369-223835419	HCPEpiC	choroid plexus:	n/a
32	chr1:223854639-223854689	HUVEC	blood vessel:	n/a
33	chr1:223835369-223835419	GM06990	blood:	n/a
34	chr1:223854704-223854754	ovcar-3	ovarian:	n/a
35	chr1:223840925-223840975	AG10803	skin:	n/a
36	chr1:223853145-223853195	SK-N-MC	brain:	n/a
37	chr1:223853928-223853978	NH-A	brain:	n/a
38	chr1:223853145-223853195	AG09319	gingival:	n/a
39	chr1:223854447-223854497	HNPCEpiC	eye:	n/a
40	chr1:223853928-223853978	SKMC	muscle:	n/a
41	chr1:223853145-223853195	HepG2	liver:	n/a
42	chr1:223854447-223854497	ProgFib	skin:	n/a
43	chr1:223840974-223841024	BJ	skin:	n/a
44	chr1:223854639-223854689	SK-N-SH_RA	brain:	n/a
45	chr1:223840925-223840975	T-47D	breast:	n/a
46	chr1:223854639-223854689	SKMC	muscle:	n/a
47	chr1:223854704-223854754	NB4	blood:	n/a
48	chr1:223854447-223854497	HEK293	kidney:	embryo
49	chr1:223853949-223853999	AG04450	lung:	fetal
50	chr1:223840974-223841024	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:223833118..223836523-chr1:223838327..223841763,4	MCF-7	breast:
2	chr1:223809528..223812099-chr1:223812404..223815945,3	K562	blood:
3	chr1:223535228..223537703-chr1:223832802..223834743,2	MCF-7	breast:
4	chr1:223825136..223827090-chr1:223853987..223856973,2	MCF-7	breast:
5	chr1:223838928..223839586-chr1:223857876..223858715,2	MCF-7	breast:
6	chr1:223836208..223847031-chr1:223849408..223858826,22	MCF-7	breast:
7	chr1:223833055..223835891-chr1:223854048..223855966,2	K562	blood:
8	chr1:223829687..223833751-chr1:223837016..223839699,4	MCF-7	breast:
9	chr1:223819090..223819750-chr1:223857938..223858740,2	MCF-7	breast:
10	chr1:223827183..223829380-chr1:223830891..223832610,2	MCF-7	breast:
11	chr1:223825136..223827090-chr1:223853987..223856973,2	MCF-7	breast:
12	chr1:223322225..223323066-chr1:223842691..223843630,2	MCF-7	breast:
13	chr1:223837812..223840547-chr1:223845364..223849589,4	K562	blood:
14	chr1:223831879..223834743-chr1:223845715..223848312,2	K562	blood:
15	chr1:223837812..223840547-chr1:223845364..223849589,4	K562	blood:
16	chr1:223815744..223816492-chr1:223826635..223827327,2	K562	blood:
17	chr1:223722935..223725716-chr1:223807910..223810771,2	MCF-7	breast:
18	chr1:223846868..223849308-chr1:223851212..223853858,2	K562	blood:
19	chr1:223827148..223829506-chr1:223840054..223841666,2	MCF-7	breast:
20	chr1:223809528..223812099-chr1:223812404..223815945,3	K562	blood:
21	chr1:223850712..223853354-chr1:223854192..223856571,2	MCF-7	breast:
22	chr1:223843142..223845522-chr1:223848017..223849601,2	K562	blood:
23	chr1:223823766..223826400-chr1:223828935..223830773,2	K562	blood:
24	chr1:223817010..223818658-chr1:223819579..223821945,2	K562	blood:
25	chr1:223840282..223843675-chr1:223851675..223856291,7	MCF-7	breast:
26	chr1:223832588..223834103-chr1:223850844..223852665,2	MCF-7	breast:
27	chr1:223826154..223828830-chr1:223841356..223843010,2	MCF-7	breast:
28	chr1:223348196..223351831-chr1:223853498..223856683,4	MCF-7	breast:
29	chr1:223843142..223845522-chr1:223848017..223849601,2	K562	blood:
30	chr1:223827325..223830055-chr1:223836590..223838294,2	MCF-7	breast:
31	chr1:223831956..223833970-chr1:223853050..223855835,2	MCF-7	breast:
32	chr1:223834427..223836360-chr1:223837595..223841642,3	MCF-7	breast:
33	chr1:223803243..223805245-chr1:223838331..223840277,2	MCF-7	breast:
34	chr1:223840282..223843675-chr1:223851675..223856291,7	MCF-7	breast:
35	chr1:223833055..223835891-chr1:223854048..223855966,2	K562	blood:
36	chr1:223832588..223834103-chr1:223850844..223852665,2	MCF-7	breast:
37	chr1:223836208..223847031-chr1:223849408..223858826,22	MCF-7	breast:
38	chr1:223823766..223826400-chr1:223828935..223830773,2	K562	blood:
39	chr1:223809178..223812919-chr1:223814445..223817998,4	K562	blood:
40	chr1:223842591..223843487-chr1:223870928..223871712,2	MCF-7	breast:
41	chr1:223827325..223830055-chr1:223836590..223838294,2	MCF-7	breast:
42	chr1:223840874..223841758-chr8:63546888..63547676,2	MCF-7	breast:
43	chr1:223853852..223855706-chr1:223946715..223948642,2	K562	blood:
44	chr1:223801253..223805310-chr1:223810350..223813712,3	K562	blood:
45	chr1:223846678..223849774-chr1:223851871..223853598,3	MCF-7	breast:
46	chr1:223802950..223805657-chr20:60696653..60698417,2	MCF-7	breast:
47	chr1:223834427..223836360-chr1:223837595..223841642,3	MCF-7	breast:
48	chr1:223801253..223805310-chr1:223810350..223813712,3	K562	blood:
49	chr1:223817010..223818658-chr1:223819579..223821945,2	K562	blood:
50	chr1:223827148..223829506-chr1:223840054..223841666,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TP53BP2-5	chr1:223831812-223832085	NONHSAT009740

Variant related genes	Relation type
SNRPEP10	TF binding region
CAPN8	TF binding region
SNRPEP10	CpG island
CAPN8	CpG island
ENSG00000143502	chromatin interactions
ENSG00000227002	chromatin interactions
ENSG00000162909	chromatin interactions
ENSG00000203697	chromatin interactions
ENSG00000149657	chromatin interactions

Extended variants
information (count: 2269 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2269 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114411900	chr1:223803556-223803557	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs115060317	chr1:223803561-223803562	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558716860	chr1:223803564-223803565	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147011499	chr1:223803619-223803620	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540967123	chr1:223803661-223803662	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559218558	chr1:223803665-223803666	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs147604672	chr1:223803680-223803681	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs369989023	chr1:223803681-223803682	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs149084097	chr1:223803689-223803690	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201966250	chr1:223803694-223803695	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs376301243	chr1:223803722-223803723	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs370802977	chr1:223803730-223803731	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs192136287	chr1:223803731-223803732	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143158249	chr1:223803747-223803748	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs571036568	chr1:223803750-223803751	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528671838	chr1:223803754-223803755	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547366334	chr1:223803780-223803781	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs568750233	chr1:223803782-223803783	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536121019	chr1:223803814-223803815	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs267598390	chr1:223803815-223803816	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200427409	chr1:223803826-223803827	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs373894809	chr1:223803843-223803844	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182699599	chr1:223803881-223803882	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs569107880	chr1:223803886-223803887	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs373424118	chr1:223803904-223803905	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375114312	chr1:223803907-223803908	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs557961727	chr1:223803921-223803922	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187124387	chr1:223803989-223803990	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192334942	chr1:223804006-223804007	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534487834	chr1:223804017-223804018	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574976064	chr1:223804032-223804033	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs184446192	chr1:223804054-223804055	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs73119721	chr1:223804095-223804096	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs541693775	chr1:223804113-223804114	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563300069	chr1:223804143-223804144	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74862134	chr1:223804144-223804145	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545926849	chr1:223804157-223804158	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs564025850	chr1:223804220-223804221	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs35497806	chr1:223804245-223804246	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs148319467	chr1:223804247-223804248	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs547201774	chr1:223804252-223804253	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562235149	chr1:223804257-223804258	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189594861	chr1:223804290-223804291	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551252900	chr1:223804354-223804355	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563832450	chr1:223804412-223804413	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs73119723	chr1:223804420-223804421	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34176751	chr1:223804458-223804459	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114991331	chr1:223804517-223804518	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551879241	chr1:223804561-223804562	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs193276365	chr1:223804619-223804620	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:503 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223796800-223811800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:223797000-223805600	Weak transcription	Lung	lung
3	chr1:223799400-223815400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr1:223799800-223806000	Weak transcription	Fetal Stomach	stomach
5	chr1:223800200-223805400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr1:223800200-223805600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr1:223800400-223805400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:223800600-223805600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr1:223802200-223804000	Strong transcription	Gastric	stomach
10	chr1:223802800-223821000	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr1:223803000-223804800	Strong transcription	Stomach Mucosa	stomach
12	chr1:223803200-223803800	Enhancers	Esophagus	oesophagus
13	chr1:223803200-223806000	Enhancers	Fetal Muscle Leg	muscle
14	chr1:223803800-223805600	Weak transcription	Esophagus	oesophagus
15	chr1:223804000-223804200	Genic enhancers	Gastric	stomach
16	chr1:223804000-223806200	Weak transcription	Fetal Intestine Small	intestine
17	chr1:223804200-223805800	Weak transcription	Gastric	stomach
18	chr1:223804800-223806800	Weak transcription	Stomach Mucosa	stomach
19	chr1:223805400-223806000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:223805400-223806000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr1:223805400-223806000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:223805400-223806200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:223805600-223805800	Strong transcription	Lung	lung
24	chr1:223805600-223806000	Enhancers	Primary hematopoietic stem cells	blood
25	chr1:223805600-223806000	Enhancers	Fetal Muscle Trunk	muscle
26	chr1:223805600-223806200	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr1:223805600-223806600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr1:223805600-223806600	Enhancers	Placenta	Placenta
29	chr1:223805600-223807200	Enhancers	Spleen	Spleen
30	chr1:223805800-223806000	Enhancers	Esophagus	oesophagus
31	chr1:223805800-223806000	Genic enhancers	Lung	lung
32	chr1:223805800-223806200	Strong transcription	Gastric	stomach
33	chr1:223805800-223806200	Bivalent Enhancer	HepG2	liver
34	chr1:223806000-223806200	Strong transcription	Lung	lung
35	chr1:223806000-223806400	Strong transcription	Fetal Stomach	stomach
36	chr1:223806000-223807200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr1:223806000-223808000	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr1:223806200-223806400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr1:223806200-223806600	Enhancers	Fetal Intestine Small	intestine
40	chr1:223806200-223807200	Genic enhancers	Gastric	stomach
41	chr1:223806200-223809200	Enhancers	HepG2	liver
42	chr1:223806200-223810200	Enhancers	Fetal Intestine Large	intestine
43	chr1:223806200-223816400	Weak transcription	Lung	lung
44	chr1:223806400-223809800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:223806400-223811800	Weak transcription	Fetal Stomach	stomach
46	chr1:223806600-223807600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr1:223806600-223808000	Weak transcription	Fetal Intestine Small	intestine
48	chr1:223806600-223808000	Weak transcription	Placenta	Placenta
49	chr1:223806800-223808200	Genic enhancers	Stomach Mucosa	stomach
50	chr1:223806800-223808800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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