Variant report

Variant	nsv513775
Chromosome Location	chr22:29083731-29137822
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	ARID3A	chr22:29137362-29138120	K562	blood:	n/a	n/a
2	ARID3A	chr22:29107841-29108771	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:29137622-29138383	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:29136182-29136698	K562	blood:	n/a	n/a
5	ATF1	chr22:29137500-29138115	K562	blood:	n/a	n/a
6	ATF2	chr22:29137595-29138099	GM12878	blood:	n/a	n/a
7	ATF3	chr22:29137593-29137980	K562	blood:	n/a	n/a
8	ATF3	chr22:29137560-29138014	K562	blood:	n/a	n/a
9	ATF3	chr22:29137694-29138015	HepG2	liver:	n/a	n/a
10	ATF3	chr22:29108352-29108738	A549	lung:	n/a	n/a
11	BACH1	chr22:29137661-29138549	H1-hESC	embryonic stem cell:	n/a	chr22:29137745-29137759
12	BATF	chr22:29088114-29088341	GM12878	blood:	n/a	n/a
13	BATF	chr22:29110082-29110388	GM12878	blood:	n/a	n/a
14	BATF	chr22:29137359-29138010	GM12878	blood:	n/a	n/a
15	BATF	chr22:29110124-29110396	GM12878	blood:	n/a	n/a
16	BATF	chr22:29084039-29084373	GM12878	blood:	n/a	n/a
17	BATF	chr22:29137452-29137909	GM12878	blood:	n/a	n/a
18	BATF	chr22:29088557-29088776	GM12878	blood:	n/a	n/a
19	BCL11A	chr22:29085983-29086182	GM12878	blood:	n/a	n/a
20	BCL11A	chr22:29088139-29088370	GM12878	blood:	n/a	chr22:29088204-29088212
21	BCL3	chr22:29108146-29108868	A549	lung:	n/a	n/a
22	BCL3	chr22:29108214-29108740	A549	lung:	n/a	n/a
23	BCLAF1	chr22:29137377-29138361	GM12878	blood:	n/a	n/a
24	BHLHE40	chr22:29137518-29138775	K562	blood:	n/a	n/a
25	BHLHE40	chr22:29137367-29138904	GM12878	blood:	n/a	n/a
26	BRCA1	chr22:29108040-29108805	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr22:29137558-29138449	Hela-S3	cervix:	n/a	chr22:29137731-29137738
28	CBX3	chr22:29137477-29137986	K562	blood:	n/a	n/a
29	CEBPB	chr22:29108296-29108728	MCF-7	breast:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539
30	CEBPB	chr22:29108079-29108362	HepG2	liver:	n/a	chr22:29108258-29108269
31	CEBPB	chr22:29104786-29105398	Hela-S3	cervix:	n/a	chr22:29105188-29105201
32	CEBPB	chr22:29108057-29108754	IMR90	lung:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539 chr22:29108258-29108269
33	CEBPB	chr22:29107889-29108729	A549	lung:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539 chr22:29108258-29108269
34	CEBPB	chr22:29108402-29108673	HepG2	liver:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539
35	CEBPB	chr22:29124585-29124959	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr22:29108257-29108827	HCT-116	colon:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539 chr22:29108258-29108269
37	CEBPB	chr22:29137452-29138019	GM12878	blood:	n/a	chr22:29138001-29138009 chr22:29137842-29137850
38	CEBPB	chr22:29108439-29108591	K562	blood:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539
39	CEBPB	chr22:29108358-29108703	H1-hESC	embryonic stem cell:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539
40	CEBPB	chr22:29107993-29108814	A549	lung:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539 chr22:29108258-29108269
41	CEBPB	chr22:29100786-29100969	HepG2	liver:	n/a	chr22:29100830-29100847 chr22:29100833-29100844
42	CEBPB	chr22:29108214-29108682	K562	blood:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539 chr22:29108258-29108269
43	CEBPB	chr22:29137475-29138073	Hela-S3	cervix:	n/a	chr22:29138001-29138009 chr22:29137842-29137850
44	CEBPB	chr22:29108293-29108780	ECC-1	luminal epithelium:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539
45	CEBPB	chr22:29108404-29108597	K562	blood:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539
46	CEBPB	chr22:29124609-29124927	IMR90	lung:	n/a	n/a
47	CEBPB	chr22:29108337-29108640	HCT-116	colon:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539
48	CEBPB	chr22:29108062-29108723	HepG2	liver:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539 chr22:29108258-29108269
49	CEBPB	chr22:29107903-29108935	A549	lung:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539 chr22:29108258-29108269
50	CEBPB	chr22:29107879-29109128	Hela-S3	cervix:	n/a	chr22:29108530-29108541 chr22:29108530-29108539 chr22:29108528-29108539 chr22:29108258-29108269

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29134743-29134793	NT2-D1	testis:	n/a
2	chr22:29134743-29134793	NT2-D1	testis:	n/a
3	chr22:29137759-29137809	Caco-2	colon:	n/a
4	chr22:29137598-29137648	Hela-S3	cervix:	n/a
5	chr22:29137759-29137809	NHDF-neo	bronchial:	n/a
6	chr22:29134743-29134793	MCF10A-Er-Src	breast:	n/a
7	chr22:29105478-29105528	HCM	heart:	n/a
8	chr22:29137527-29137577	NH-A	brain:	n/a
9	chr22:29137527-29137577	AoSMC	blood vessel:	n/a
10	chr22:29137598-29137648	IMR90	lung:	fetal
11	chr22:29105478-29105528	HEEpiC	esophagus:	n/a
12	chr22:29137759-29137809	HCM	heart:	n/a
13	chr22:29134743-29134793	HIPEpiC	eye:	n/a
14	chr22:29136685-29136735	AG04450	lung:	fetal
15	chr22:29134743-29134793	AG04450	lung:	fetal
16	chr22:29136685-29136735	HL-60	blood:	n/a
17	chr22:29137527-29137577	HRE	kidney:	n/a
18	chr22:29105478-29105528	BJ	skin:	n/a
19	chr22:29137527-29137577	PrEC	prostate:	n/a
20	chr22:29136685-29136735	CMK	blood:	n/a
21	chr22:29136685-29136735	SK-N-MC	brain:	n/a
22	chr22:29105478-29105528	NHDF-neo	bronchial:	n/a
23	chr22:29137527-29137577	SKMC	muscle:	n/a
24	chr22:29137598-29137648	HUVEC	blood vessel:	n/a
25	chr22:29105478-29105528	RPTEC	kidney:	n/a
26	chr22:29137527-29137577	NB4	blood:	n/a
27	chr22:29137527-29137577	BE2_C	brain:	n/a
28	chr22:29137527-29137577	SK-N-SH	brain:	n/a
29	chr22:29105478-29105528	MCF-7	breast:	n/a
30	chr22:29134743-29134793	CMK	blood:	n/a
31	chr22:29105478-29105528	NT2-D1	testis:	n/a
32	chr22:29105478-29105528	HRPEpiC	eye:	n/a
33	chr22:29105478-29105528	CMK	blood:	n/a
34	chr22:29137598-29137648	HMEC	breast:	n/a
35	chr22:29137598-29137648	NT2-D1	testis:	n/a
36	chr22:29136685-29136735	HEK293	kidney:	embryo
37	chr22:29137527-29137577	AG09319	gingival:	n/a
38	chr22:29134743-29134793	A549	lung:	n/a
39	chr22:29137527-29137577	Hepatocyte	liver:	n/a
40	chr22:29137598-29137648	ProgFib	skin:	n/a
41	chr22:29137598-29137648	CMK	blood:	n/a
42	chr22:29137759-29137809	SK-N-MC	brain:	n/a
43	chr22:29105478-29105528	HepG2	liver:	n/a
44	chr22:29136685-29136735	SKMC	muscle:	n/a
45	chr22:29105478-29105528	SKMC	muscle:	n/a
46	chr22:29137759-29137809	U87	brain:	n/a
47	chr22:29105478-29105528	AG04449	skin:	fetal
48	chr22:29137759-29137809	AoSMC	blood vessel:	n/a
49	chr22:29134743-29134793	Hepatocyte	liver:	n/a
50	chr22:29136685-29136735	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:29137399..29139735-chr22:29278518..29281229,2	MCF-7	breast:
2	chr22:29136431..29140671-chr22:29167494..29170117,5	K562	blood:
3	chr22:29133133..29134961-chr22:29136110..29137715,2	K562	blood:
4	chr22:29098731..29101679-chr22:29195064..29196979,2	MCF-7	breast:
5	chr22:29133437..29141650-chr22:29203240..29216422,34	MCF-7	breast:
6	chr22:29123587..29125370-chr22:29195302..29198150,2	MCF-7	breast:
7	chr22:29117174..29121072-chr22:29214167..29218660,4	MCF-7	breast:
8	chr22:29093925..29096043-chr22:29097734..29099299,2	K562	blood:
9	chr22:29094612..29096688-chr22:29136318..29138280,2	K562	blood:
10	chr22:29137732..29138603-chr9:127962252..127962851,2	Hela-S3	cervix:
11	chr22:29106300..29106832-chr6:153441688..153442188,2	Hela-S3	cervix:
12	chr22:29126583..29142031-chr22:29203252..29220632,67	MCF-7	breast:
13	chr14:24681489..24683896-chr22:29136971..29139325,2	MCF-7	breast:
14	chr22:29098955..29101024-chr22:29190318..29193070,2	K562	blood:
15	chr22:29124921..29127441-chr22:29136398..29138709,2	K562	blood:
16	chr22:29116498..29119030-chr22:29122094..29124064,2	MCF-7	breast:
17	chr22:29093925..29096043-chr22:29097734..29099299,2	K562	blood:
18	chr22:29134319..29139472-chr22:29186598..29194420,8	K562	blood:
19	chr22:29129415..29131675-chr22:29131863..29134375,2	MCF-7	breast:
20	chr22:29137681..29138362-chr22:29196436..29197177,2	MCF-7	breast:
21	chr22:29134224..29141746-chr22:29191206..29200044,27	MCF-7	breast:
22	chr22:29137710..29139572-chr22:29196791..29200014,3	K562	blood:
23	chr22:29134226..29139597-chr22:29164663..29170736,9	K562	blood:
24	chr22:29103207..29105613-chr22:29137554..29139656,2	MCF-7	breast:
25	chr22:29134212..29140528-chr22:29167074..29172462,20	MCF-7	breast:
26	chr22:29090716..29093047-chr22:29154418..29156765,2	K562	blood:
27	chr22:29121818..29125415-chr22:29136327..29139061,3	MCF-7	breast:
28	chr22:29135038..29141691-chr22:29167545..29172967,16	MCF-7	breast:
29	chr22:29117650..29119944-chr22:29134388..29136343,2	MCF-7	breast:
30	chr15:67813222..67814078-chr22:29137791..29138574,2	Hela-S3	cervix:
31	chr22:29137011..29139217-chr22:29662922..29665353,2	MCF-7	breast:
32	chr22:29117650..29119944-chr22:29134388..29136343,2	MCF-7	breast:
33	chr22:29133133..29134961-chr22:29136110..29137715,2	K562	blood:
34	chr22:29133124..29135770-chr22:29178990..29181478,2	MCF-7	breast:
35	chr16:87350540..87351128-chr22:29137773..29138461,2	Hela-S3	cervix:
36	chr22:29131911..29134961-chr22:29136110..29138842,3	K562	blood:
37	chr22:29116498..29119030-chr22:29122094..29124064,2	MCF-7	breast:
38	chr22:29124921..29127441-chr22:29136398..29138709,2	K562	blood:
39	chr22:29123719..29125276-chr22:29194565..29196518,3	MCF-7	breast:
40	chr22:29118802..29121164-chr22:29193533..29196083,2	MCF-7	breast:
41	chr17:58153269..58156234-chr22:29137752..29139520,2	MCF-7	breast:
42	chr22:29127658..29141630-chr22:29187451..29201381,67	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC28-1	chr22:29083737-29083974	NONHSAT084651
2	lnc-TTC28-1	chr22:29085123-29085398	NONHSAT084651

Variant related genes	Relation type
CHEK2	TF binding region
HSCB	TF binding region
CHEK2	CpG island
HSCB	CpG island
ENSG00000159873	chromatin interactions
ENSG00000189227	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000260456	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000259673	chromatin interactions
ENSG00000136933	chromatin interactions
ENSG00000183579	chromatin interactions
ENSG00000100263	chromatin interactions
ENSG00000270006	chromatin interactions
ENSG00000183765	chromatin interactions
ENSG00000254505	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000182944	chromatin interactions
ENSG00000272858	chromatin interactions
ENSG00000068097	chromatin interactions
ENSG00000254692	chromatin interactions

Extended variants
information (count: 2184 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2184 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541513166	chr22:29083808-29083809	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs540410451	chr22:29083826-29083827	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs562206743	chr22:29083843-29083844	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs529320954	chr22:29083856-29083857	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs17884403	chr22:29083867-29083868	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs121908710	chr22:29083878-29083879	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs17886242	chr22:29083909-29083910	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs544216926	chr22:29083913-29083914	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs576248104	chr22:29083914-29083915	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs562517792	chr22:29083920-29083921	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs138040612	chr22:29083935-29083936	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs149501505	chr22:29083950-29083951	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs202104749	chr22:29083951-29083952	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs373959274	chr22:29083955-29083956	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs533475838	chr22:29083956-29083957	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs200432447	chr22:29083962-29083963	Strong transcription Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs551645416	chr22:29083994-29083995	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs121908709	chr22:29084005-29084006	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367844311	chr22:29084022-29084023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs17880159	chr22:29084052-29084053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111711838	chr22:29084059-29084060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188451595	chr22:29084073-29084074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200886654	chr22:29084120-29084121	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527883495	chr22:29084127-29084128	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549265457	chr22:29084137-29084138	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17881275	chr22:29084142-29084143	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17880568	chr22:29084166-29084167	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs370515134	chr22:29084182-29084183	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373632645	chr22:29084210-29084211	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571241511	chr22:29084211-29084212	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192274133	chr22:29084231-29084232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs182964430	chr22:29084247-29084248	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572191260	chr22:29084248-29084249	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542807862	chr22:29084326-29084327	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554426567	chr22:29084342-29084343	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368704747	chr22:29084359-29084360	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113712283	chr22:29084360-29084361	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139467994	chr22:29084385-29084386	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62235682	chr22:29084417-29084418	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562580577	chr22:29084422-29084423	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577607974	chr22:29084455-29084456	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545341192	chr22:29084459-29084460	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62235683	chr22:29084486-29084487	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77090246	chr22:29084501-29084502	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560843072	chr22:29084548-29084549	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527940093	chr22:29084588-29084589	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149014632	chr22:29084594-29084595	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559259853	chr22:29084626-29084627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575333671	chr22:29084627-29084628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531461943	chr22:29084659-29084660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20616022	CNVD
Breast cancer	21486468	CNVD
Ovarian cancer	21486468	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1390 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29076200-29089200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr22:29076200-29103000	Weak transcription	GM12878-XiMat	blood
3	chr22:29076200-29137600	Weak transcription	Esophagus	oesophagus
4	chr22:29076400-29084200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr22:29076400-29085200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr22:29076400-29085400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr22:29076400-29085800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr22:29076400-29088400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr22:29076400-29088600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr22:29076400-29092800	Weak transcription	Primary B cells from cord blood	blood
11	chr22:29076400-29098000	Weak transcription	Ovary	ovary
12	chr22:29076400-29099400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr22:29076400-29102000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr22:29076400-29103000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr22:29076400-29105000	Weak transcription	HUVEC	blood vessel
16	chr22:29076400-29105200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr22:29076400-29105800	Weak transcription	NHLF	lung
18	chr22:29076400-29119200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr22:29076400-29129400	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr22:29076600-29085200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr22:29076600-29089400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr22:29076600-29094400	Weak transcription	Fetal Muscle Trunk	muscle
23	chr22:29076600-29102200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr22:29077200-29105000	Weak transcription	Osteobl	bone
25	chr22:29077400-29102000	Weak transcription	Fetal Intestine Large	intestine
26	chr22:29077400-29106000	Weak transcription	A549	lung
27	chr22:29077600-29099000	Weak transcription	Hela-S3	cervix
28	chr22:29077600-29102800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr22:29079000-29089200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr22:29079600-29130200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr22:29079800-29089200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr22:29079800-29089200	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr22:29080200-29087200	Weak transcription	Fetal Intestine Small	intestine
34	chr22:29080600-29092000	Weak transcription	NHEK	skin
35	chr22:29081200-29089400	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr22:29081600-29089200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr22:29082200-29086400	Strong transcription	Fetal Stomach	stomach
38	chr22:29082200-29109800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr22:29082400-29083800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr22:29082600-29084000	Strong transcription	H1 Cell Line	embryonic stem cell
41	chr22:29082600-29084000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr22:29082600-29086000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr22:29082600-29089200	Weak transcription	Duodenum Mucosa	Duodenum
44	chr22:29082600-29092200	Weak transcription	Primary hematopoietic stem cells	blood
45	chr22:29082800-29084000	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr22:29082800-29092000	Weak transcription	HepG2	liver
47	chr22:29082800-29106000	Weak transcription	Liver	Liver
48	chr22:29082800-29137600	Weak transcription	Spleen	Spleen
49	chr22:29083000-29084400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr22:29083000-29089400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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