Variant report

Variant	nsv873212
Chromosome Location	chr1:223807262-223853792
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	ATF3	chr1:223816000-223816218	K562	blood:	n/a	n/a
2	BACH1	chr1:223834947-223834971	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr1:223808049-223808372	GM12878	blood:	n/a	chr1:223808205-223808216
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	BCL11A	chr1:223809058-223809350	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:223808999-223809391	GM12878	blood:	n/a	n/a
9	BCL3	chr1:223842759-223843334	A549	lung:	n/a	n/a
10	BCL3	chr1:223809039-223809430	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:223815889-223816261	K562	blood:	n/a	n/a
12	BHLHE40	chr1:223809040-223809519	GM12878	blood:	n/a	n/a
13	CBX3	chr1:223815860-223816359	K562	blood:	n/a	n/a
14	CEBPB	chr1:223840146-223840530	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:223851839-223852173	Hela-S3	cervix:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
16	CEBPB	chr1:223851859-223852168	H1-hESC	embryonic stem cell:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
17	CEBPB	chr1:223851845-223852146	ECC-1	luminal epithelium:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
18	CEBPB	chr1:223842598-223843268	MCF-7	breast:	n/a	n/a
19	CEBPB	chr1:223825571-223825761	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:223826960-223827254	A549	lung:	n/a	chr1:223827097-223827108
21	CEBPB	chr1:223826953-223827268	K562	blood:	n/a	chr1:223827097-223827108
22	CEBPB	chr1:223851716-223852214	MCF-7	breast:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
23	CEBPB	chr1:223826932-223827280	Hela-S3	cervix:	n/a	chr1:223827097-223827108
24	CEBPB	chr1:223844841-223844933	HepG2	liver:	n/a	chr1:223844867-223844880 chr1:223844866-223844883 chr1:223844867-223844880
25	CEBPB	chr1:223851676-223852259	A549	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
26	CEBPB	chr1:223826966-223827207	HepG2	liver:	n/a	chr1:223827097-223827108
27	CEBPB	chr1:223826873-223827448	MCF-7	breast:	n/a	chr1:223827097-223827108
28	CEBPB	chr1:223851734-223852179	MCF-7	breast:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
29	CEBPB	chr1:223812732-223812865	K562	blood:	n/a	n/a
30	CEBPB	chr1:223851818-223852190	A549	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
31	CEBPB	chr1:223851821-223852161	K562	blood:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
32	CEBPB	chr1:223822220-223822370	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:223826952-223827252	K562	blood:	n/a	chr1:223827097-223827108
34	CEBPB	chr1:223851866-223852042	HepG2	liver:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
35	CEBPB	chr1:223851813-223852188	HepG2	liver:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
36	CEBPB	chr1:223851815-223852192	K562	blood:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
37	CEBPB	chr1:223835053-223835253	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr1:223851805-223852209	A549	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
39	CEBPB	chr1:223851823-223852172	IMR90	lung:	n/a	chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004 chr1:223851995-223852004
40	CEBPB	chr1:223826848-223827494	MCF-7	breast:	n/a	chr1:223827097-223827108
41	CHD2	chr1:223809987-223810219	HepG2	liver:	n/a	n/a
42	CREB1	chr1:223841773-223842325	A549	lung:	n/a	n/a
43	CREB1	chr1:223809010-223809535	GM12878	blood:	n/a	n/a
44	CTCF	chr1:223815807-223816452	SK-N-SH	brain:	n/a	chr1:223816071-223816078 chr1:223816066-223816079 chr1:223816065-223816081 chr1:223816066-223816079 chr1:223816059-223816080 chr1:223816064-223816082 chr1:223815903-223815912
45	CTCF	chr1:223815843-223815844	NHEK	skin:	n/a	n/a
46	CTCF	chr1:223815937-223816216	MCF-7	breast:	n/a	chr1:223816071-223816078 chr1:223816066-223816079 chr1:223816065-223816081 chr1:223816066-223816079 chr1:223816059-223816080 chr1:223816064-223816082
47	CTCF	chr1:223841740-223841890	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:223815740-223815825	GM10248	blood:	n/a	n/a
49	CTCF	chr1:223816060-223816210	AoAF	blood vessel:	n/a	chr1:223816071-223816078 chr1:223816066-223816079 chr1:223816065-223816081 chr1:223816066-223816079 chr1:223816064-223816082
50	CTCF	chr1:223815940-223816090	HFF-Myc	foreskin:	n/a	chr1:223816071-223816078 chr1:223816066-223816079 chr1:223816065-223816081 chr1:223816066-223816079 chr1:223816059-223816080 chr1:223816064-223816082

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:223840925-223840975	Caco-2	colon:	n/a
2	chr1:223840974-223841024	CMK	blood:	n/a
3	chr1:223840925-223840975	Caco-2	colon:	n/a
4	chr1:223840974-223841024	CMK	blood:	n/a
5	chr1:223840925-223840975	GM12891	blood:	n/a
6	chr1:223853145-223853195	SK-N-SH	brain:	n/a
7	chr1:223840925-223840975	NB4	blood:	n/a
8	chr1:223840925-223840975	H1-hESC	embryonic stem cell:	embryo
9	chr1:223840974-223841024	H1-hESC	embryonic stem cell:	embryo
10	chr1:223853145-223853195	BJ	skin:	n/a
11	chr1:223840925-223840975	MCF-7	breast:	n/a
12	chr1:223840925-223840975	SKMC	muscle:	n/a
13	chr1:223853145-223853195	GM19239	blood:	n/a
14	chr1:223835369-223835419	AG09319	gingival:	n/a
15	chr1:223853145-223853195	HCM	heart:	n/a
16	chr1:223835369-223835419	NT2-D1	testis:	n/a
17	chr1:223840925-223840975	HepG2	liver:	n/a
18	chr1:223853145-223853195	AoSMC	blood vessel:	n/a
19	chr1:223840925-223840975	HMEC	breast:	n/a
20	chr1:223840974-223841024	HAEpiC	amniotic membrane:	n/a
21	chr1:223853145-223853195	A549	lung:	n/a
22	chr1:223840974-223841024	HIPEpiC	eye:	n/a
23	chr1:223853145-223853195	U87	brain:	n/a
24	chr1:223835369-223835419	SK-N-SH_RA	brain:	n/a
25	chr1:223835369-223835419	PFSK-1	brain:	n/a
26	chr1:223853145-223853195	ECC-1	luminal epithelium:	n/a
27	chr1:223835369-223835419	SKMC	muscle:	n/a
28	chr1:223840974-223841024	HCF	heart:	n/a
29	chr1:223835369-223835419	ECC-1	luminal epithelium:	n/a
30	chr1:223840974-223841024	AoSMC	blood vessel:	n/a
31	chr1:223840925-223840975	GM12878	blood:	n/a
32	chr1:223853145-223853195	H1-hESC	embryonic stem cell:	embryo
33	chr1:223840925-223840975	BJ	skin:	n/a
34	chr1:223853145-223853195	HIPEpiC	eye:	n/a
35	chr1:223840925-223840975	NHDF-neo	bronchial:	n/a
36	chr1:223835369-223835419	HCM	heart:	n/a
37	chr1:223853145-223853195	ovcar-3	ovarian:	n/a
38	chr1:223840974-223841024	SAEC	small airway:	n/a
39	chr1:223840925-223840975	HRCEpiC	kidney:	n/a
40	chr1:223835369-223835419	NH-A	brain:	n/a
41	chr1:223840974-223841024	BE2_C	brain:	n/a
42	chr1:223853145-223853195	HepG2	liver:	n/a
43	chr1:223840974-223841024	IMR90	lung:	fetal
44	chr1:223853145-223853195	SK-N-MC	brain:	n/a
45	chr1:223840925-223840975	MCF10A-Er-Src	breast:	n/a
46	chr1:223853145-223853195	Hela-S3	cervix:	n/a
47	chr1:223840974-223841024	NHDF-neo	bronchial:	n/a
48	chr1:223840925-223840975	LNCaP	prostate:	n/a
49	chr1:223835369-223835419	H1-hESC	embryonic stem cell:	embryo
50	chr1:223840974-223841024	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:223837812..223840547-chr1:223845364..223849589,4	K562	blood:
2	chr1:223831956..223833970-chr1:223853050..223855835,2	MCF-7	breast:
3	chr1:223803243..223805245-chr1:223838331..223840277,2	MCF-7	breast:
4	chr1:223827148..223829506-chr1:223840054..223841666,2	MCF-7	breast:
5	chr1:223840874..223841758-chr8:63546888..63547676,2	MCF-7	breast:
6	chr1:223836208..223847031-chr1:223849408..223858826,22	MCF-7	breast:
7	chr1:223832588..223834103-chr1:223850844..223852665,2	MCF-7	breast:
8	chr1:223817010..223818658-chr1:223819579..223821945,2	K562	blood:
9	chr1:223815744..223818238-chr1:223828274..223830462,2	K562	blood:
10	chr1:223322225..223323066-chr1:223842691..223843630,2	MCF-7	breast:
11	chr1:223348196..223351831-chr1:223853498..223856683,4	MCF-7	breast:
12	chr1:223836208..223847031-chr1:223849408..223858826,22	MCF-7	breast:
13	chr1:223819090..223819750-chr1:223857938..223858740,2	MCF-7	breast:
14	chr1:223846678..223849774-chr1:223851871..223853598,3	MCF-7	breast:
15	chr1:223817010..223818658-chr1:223819579..223821945,2	K562	blood:
16	chr1:223829687..223833751-chr1:223837016..223839699,4	MCF-7	breast:
17	chr1:223827325..223830055-chr1:223836590..223838294,2	MCF-7	breast:
18	chr1:223842591..223843487-chr1:223870928..223871712,2	MCF-7	breast:
19	chr1:223833118..223836523-chr1:223838327..223841763,4	MCF-7	breast:
20	chr1:223827148..223829506-chr1:223840054..223841666,2	MCF-7	breast:
21	chr1:223832588..223834103-chr1:223850844..223852665,2	MCF-7	breast:
22	chr1:223809178..223812919-chr1:223814445..223817998,4	K562	blood:
23	chr1:223840282..223843675-chr1:223851675..223856291,7	MCF-7	breast:
24	chr1:223834427..223836360-chr1:223837595..223841642,3	MCF-7	breast:
25	chr1:223843142..223845522-chr1:223848017..223849601,2	K562	blood:
26	chr1:223823766..223826400-chr1:223828935..223830773,2	K562	blood:
27	chr1:223801253..223805310-chr1:223810350..223813712,3	K562	blood:
28	chr1:223831956..223833970-chr1:223853050..223855835,2	MCF-7	breast:
29	chr1:223833118..223836523-chr1:223838327..223841763,4	MCF-7	breast:
30	chr1:223809528..223812099-chr1:223812404..223815945,3	K562	blood:
31	chr1:223834427..223836360-chr1:223837595..223841642,3	MCF-7	breast:
32	chr1:223827325..223830055-chr1:223836590..223838294,2	MCF-7	breast:
33	chr1:223815744..223816492-chr1:223826635..223827327,2	K562	blood:
34	chr1:223809528..223812099-chr1:223812404..223815945,3	K562	blood:
35	chr1:223535228..223537703-chr1:223832802..223834743,2	MCF-7	breast:
36	chr1:223838928..223839586-chr1:223857876..223858715,2	MCF-7	breast:
37	chr1:223837812..223840547-chr1:223845364..223849589,4	K562	blood:
38	chr1:223831879..223834743-chr1:223845715..223848312,2	K562	blood:
39	chr1:223846868..223849308-chr1:223851212..223853858,2	K562	blood:
40	chr1:223840282..223843675-chr1:223851675..223856291,7	MCF-7	breast:
41	chr1:223826154..223828830-chr1:223841356..223843010,2	MCF-7	breast:
42	chr1:223825136..223827090-chr1:223853987..223856973,2	MCF-7	breast:
43	chr1:223823766..223826400-chr1:223828935..223830773,2	K562	blood:
44	chr1:223827183..223829380-chr1:223830891..223832610,2	MCF-7	breast:
45	chr1:223722935..223725716-chr1:223807910..223810771,2	MCF-7	breast:
46	chr1:223843142..223845522-chr1:223848017..223849601,2	K562	blood:
47	chr1:223833055..223835891-chr1:223854048..223855966,2	K562	blood:

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
ENSG00000203697	chromatin interactions
ENSG00000143502	chromatin interactions
ENSG00000227002	chromatin interactions

Extended variants
information (count: 2037 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:2037 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34900680	chr1:223807262-223807263	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536423665	chr1:223807335-223807336	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554995876	chr1:223807390-223807391	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570343453	chr1:223807420-223807421	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537318343	chr1:223807428-223807429	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558912815	chr1:223807457-223807458	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577267674	chr1:223807509-223807510	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566092455	chr1:223807514-223807515	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75988987	chr1:223807522-223807523	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35600877	chr1:223807589-223807590	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs34186371	chr1:223807593-223807594	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs145073519	chr1:223807729-223807730	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191720729	chr1:223807731-223807732	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs116220659	chr1:223807744-223807745	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543306972	chr1:223807753-223807754	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564907599	chr1:223807781-223807782	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552955019	chr1:223807791-223807792	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370490760	chr1:223807798-223807799	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547116470	chr1:223807799-223807800	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367606829	chr1:223807841-223807842	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147641174	chr1:223807851-223807852	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182577363	chr1:223807861-223807862	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs375599665	chr1:223807870-223807871	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537757795	chr1:223807871-223807872	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140898952	chr1:223807885-223807886	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570906133	chr1:223807893-223807894	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534996030	chr1:223807903-223807904	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372504407	chr1:223807924-223807925	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs150136459	chr1:223807940-223807941	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs575003479	chr1:223807970-223807971	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535552499	chr1:223807991-223807992	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs554754996	chr1:223807999-223808000	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576118187	chr1:223808059-223808060	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs543743977	chr1:223808066-223808067	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs145574158	chr1:223808072-223808073	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs560972188	chr1:223808116-223808117	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs148948002	chr1:223808119-223808120	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558895243	chr1:223808120-223808121	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188675944	chr1:223808129-223808130	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs74145935	chr1:223808140-223808141	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs34961910	chr1:223808147-223808148	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs563947118	chr1:223808153-223808154	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372374715	chr1:223808157-223808158	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs79125992	chr1:223808180-223808181	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs571146024	chr1:223808291-223808292	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535302996	chr1:223808298-223808299	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547040781	chr1:223808299-223808300	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577551266	chr1:223808309-223808310	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568419489	chr1:223808316-223808317	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535957225	chr1:223808459-223808460	Weak transcription Enhancers Bivalent Enhancer	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:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:223796800-223811800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:223799400-223815400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr1:223802800-223821000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr1:223806000-223808000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr1:223806200-223809200	Enhancers	HepG2	liver
6	chr1:223806200-223810200	Enhancers	Fetal Intestine Large	intestine
7	chr1:223806200-223816400	Weak transcription	Lung	lung
8	chr1:223806400-223809800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr1:223806400-223811800	Weak transcription	Fetal Stomach	stomach
10	chr1:223806600-223807600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr1:223806600-223808000	Weak transcription	Fetal Intestine Small	intestine
12	chr1:223806600-223808000	Weak transcription	Placenta	Placenta
13	chr1:223806800-223808200	Genic enhancers	Stomach Mucosa	stomach
14	chr1:223806800-223808800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:223807000-223807400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:223807000-223810800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:223807200-223808000	Weak transcription	Gastric	stomach
18	chr1:223807200-223808000	Weak transcription	Spleen	Spleen
19	chr1:223807400-223807800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:223807600-223810200	Enhancers	Liver	Liver
21	chr1:223807600-223810600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:223807800-223808000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:223807800-223808000	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr1:223807800-223810400	Enhancers	Fetal Muscle Leg	muscle
25	chr1:223808000-223808200	Enhancers	Placenta	Placenta
26	chr1:223808000-223808200	Genic enhancers	Gastric	stomach
27	chr1:223808000-223808200	Enhancers	Spleen	Spleen
28	chr1:223808000-223808600	Enhancers	Brain Substantia Nigra	brain
29	chr1:223808000-223808600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr1:223808000-223808600	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr1:223808000-223808600	Bivalent Enhancer	K562	blood
32	chr1:223808000-223808800	Enhancers	Fetal Intestine Small	intestine
33	chr1:223808000-223809800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr1:223808000-223809800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr1:223808000-223810200	Enhancers	Fetal Muscle Trunk	muscle
36	chr1:223808200-223808400	Weak transcription	Gastric	stomach
37	chr1:223808200-223808400	Enhancers	Pancreas	Pancrea
38	chr1:223808200-223809200	Enhancers	Stomach Mucosa	stomach
39	chr1:223808400-223808600	Enhancers	Gastric	stomach
40	chr1:223808400-223808600	Bivalent Enhancer	GM12878-XiMat	blood
41	chr1:223808400-223809000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr1:223808400-223809400	Weak transcription	Pancreas	Pancrea
43	chr1:223808600-223808800	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr1:223808600-223809000	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr1:223808600-223809600	Enhancers	GM12878-XiMat	blood
46	chr1:223808600-223825000	Weak transcription	Gastric	stomach
47	chr1:223808800-223809800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:223808800-223809800	Weak transcription	Fetal Intestine Small	intestine
49	chr1:223808800-223810800	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr1:223809000-223809400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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