Variant report

Variant	nsv532586
Chromosome Location	chr1:169593222-169713184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:857)
CpG islands
(count:1160)
Chromatin interactive
region (count:45)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:169680921-169681465	HepG2	liver:	n/a	n/a
2	ATF1	chr1:169701176-169701185	K562	blood:	n/a	n/a
3	ATF2	chr1:169666839-169667373	GM12878	blood:	n/a	n/a
4	BATF	chr1:169668150-169668460	GM12878	blood:	n/a	n/a
5	BATF	chr1:169666902-169667269	GM12878	blood:	n/a	n/a
6	BCLAF1	chr1:169680636-169681479	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:169661404-169662555	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:169658708-169658717	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:169651335-169651677	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:169681194-169681394	K562	blood:	n/a	n/a
11	BRCA1	chr1:169659659-169660100	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr1:169603412-169603713	K562	blood:	n/a	n/a
13	CBX3	chr1:169604174-169604411	K562	blood:	n/a	n/a
14	CBX3	chr1:169603444-169603824	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:169603411-169603682	K562	blood:	n/a	n/a
16	CBX3	chr1:169604174-169604539	HCT-116	colon:	n/a	n/a
17	CEBPB	chr1:169695403-169695746	K562	blood:	n/a	n/a
18	CEBPB	chr1:169710323-169710673	MCF-7	breast:	n/a	n/a
19	CEBPB	chr1:169695377-169695730	HCT-116	colon:	n/a	n/a
20	CEBPB	chr1:169695403-169695719	MCF-7	breast:	n/a	n/a
21	CEBPB	chr1:169695487-169695688	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr1:169644998-169645270	A549	lung:	n/a	chr1:169645097-169645108
23	CEBPB	chr1:169695408-169695720	A549	lung:	n/a	n/a
24	CEBPB	chr1:169695414-169695763	K562	blood:	n/a	n/a
25	CEBPB	chr1:169710187-169710749	MCF-7	breast:	n/a	n/a
26	CEBPB	chr1:169648965-169648998	K562	blood:	n/a	n/a
27	CEBPB	chr1:169645070-169645323	IMR90	lung:	n/a	chr1:169645097-169645108
28	CEBPB	chr1:169695481-169695743	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr1:169680684-169681360	GM12878	blood:	n/a	n/a
30	CHD1	chr1:169663513-169663645	GM12878	blood:	n/a	n/a
31	CHD2	chr1:169680659-169681482	GM12878	blood:	n/a	n/a
32	CHD2	chr1:169632078-169632112	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr1:169681280-169681430	HPAF	blood vessel:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
34	CTCF	chr1:169680827-169680994	K562	blood:	n/a	n/a
35	CTCF	chr1:169663480-169663630	GM12872	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
36	CTCF	chr1:169663560-169663710	GM12872	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588
37	CTCF	chr1:169680504-169681679	HCT-116	colon:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
38	CTCF	chr1:169681280-169681430	HMEC	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
39	CTCF	chr1:169680712-169681598	MCF-7	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
40	CTCF	chr1:169669046-169669203	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr1:169681145-169681521	Lung_OC	lung:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
42	CTCF	chr1:169680860-169681010	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr1:169680840-169680990	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr1:169681239-169681467	MCF-7	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
45	CTCF	chr1:169681300-169681450	HMEC	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
46	CTCF	chr1:169680820-169680970	RPTEC	kidney:	n/a	n/a
47	CTCF	chr1:169681280-169681430	HRPEpiC	eye:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
48	CTCF	chr1:169680772-169681009	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:169680788-169680950	A549	lung:	n/a	n/a
50	CTCF	chr1:169663440-169663590	GM12878	blood:	n/a	chr1:169663577-169663585 chr1:169663572-169663590 chr1:169663567-169663588

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169681427-169681477	RPTEC	kidney:	n/a
2	chr1:169681427-169681477	RPTEC	kidney:	n/a
3	chr1:169703422-169703472	ovcar-3	ovarian:	n/a
4	chr1:169630505-169630555	HAEpiC	amniotic membrane:	n/a
5	chr1:169702841-169702891	ovcar-3	ovarian:	n/a
6	chr1:169660219-169660269	SK-N-MC	brain:	n/a
7	chr1:169702841-169702891	HIPEpiC	eye:	n/a
8	chr1:169693534-169693584	HRCEpiC	kidney:	n/a
9	chr1:169599558-169599608	HRE	kidney:	n/a
10	chr1:169702841-169702891	BJ	skin:	n/a
11	chr1:169600704-169600754	AG04450	lung:	fetal
12	chr1:169631737-169631787	HCM	heart:	n/a
13	chr1:169599212-169599262	PrEC	prostate:	n/a
14	chr1:169660219-169660269	ECC-1	luminal epithelium:	n/a
15	chr1:169671116-169671166	AG10803	skin:	n/a
16	chr1:169599558-169599608	IMR90	lung:	fetal
17	chr1:169680613-169680663	BJ	skin:	n/a
18	chr1:169599212-169599262	HRCEpiC	kidney:	n/a
19	chr1:169599558-169599608	MCF-7	breast:	n/a
20	chr1:169693534-169693584	HAEpiC	amniotic membrane:	n/a
21	chr1:169671116-169671166	Hepatocyte	liver:	n/a
22	chr1:169671116-169671166	NT2-D1	testis:	n/a
23	chr1:169599212-169599262	AG04449	skin:	fetal
24	chr1:169702841-169702891	HCT-116	colon:	n/a
25	chr1:169660219-169660269	HCM	heart:	n/a
26	chr1:169681333-169681383	GM12891	blood:	n/a
27	chr1:169631737-169631787	HEEpiC	esophagus:	n/a
28	chr1:169599754-169599804	HepG2	liver:	n/a
29	chr1:169680613-169680663	SK-N-SH_RA	brain:	n/a
30	chr1:169630520-169630570	GM06990	blood:	n/a
31	chr1:169702841-169702891	GM12891	blood:	n/a
32	chr1:169631737-169631787	HRCEpiC	kidney:	n/a
33	chr1:169702841-169702891	MCF-7	breast:	n/a
34	chr1:169631737-169631787	HRE	kidney:	n/a
35	chr1:169599558-169599608	HCM	heart:	n/a
36	chr1:169599558-169599608	AG09319	gingival:	n/a
37	chr1:169630520-169630570	NHDF-neo	bronchial:	n/a
38	chr1:169599212-169599262	HCM	heart:	n/a
39	chr1:169703232-169703282	HepG2	liver:	n/a
40	chr1:169631737-169631787	AoSMC	blood vessel:	n/a
41	chr1:169702841-169702891	GM19239	blood:	n/a
42	chr1:169681333-169681383	HMEC	breast:	n/a
43	chr1:169660219-169660269	HIPEpiC	eye:	n/a
44	chr1:169630520-169630570	HIPEpiC	eye:	n/a
45	chr1:169703422-169703472	NHDF-neo	bronchial:	n/a
46	chr1:169693534-169693584	HCT-116	colon:	n/a
47	chr1:169679199-169679249	SK-N-SH	brain:	n/a
48	chr1:169600704-169600754	GM12892	blood:	n/a
49	chr1:169599558-169599608	A549	lung:	n/a
50	chr1:169703422-169703472	HEEpiC	esophagus:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:168572840..168573443-chr1:169680986..169681557,2	MCF-7	breast:
2	chr1:169680417..169682445-chr1:169762164..169765185,3	MCF-7	breast:
3	chr1:169614149..169618118-chr1:169618692..169623523,5	K562	blood:
4	chr1:169705648..169707388-chr1:169710933..169712519,2	MCF-7	breast:
5	chr1:169680922..169681530-chr1:169748582..169749325,2	MCF-7	breast:
6	chr1:169708800..169711627-chr1:169714928..169717201,2	MCF-7	breast:
7	chr1:169614149..169617850-chr1:169618797..169622086,4	K562	blood:
8	chr1:169695880..169697994-chr1:169699455..169701036,2	MCF-7	breast:
9	chr1:169569836..169571238-chr1:169680901..169681521,6	MCF-7	breast:
10	chr1:169669179..169671320-chr1:169675894..169677671,2	K562	blood:
11	chr1:169705648..169707388-chr1:169710933..169712519,2	MCF-7	breast:
12	chr1:169679878..169683283-chr1:169762041..169765464,5	MCF-7	breast:
13	chr1:169708422..169710485-chr1:169860930..169862840,2	MCF-7	breast:
14	chr1:169707608..169709249-chr1:169711620..169714505,2	MCF-7	breast:
15	chr1:168572487..168573340-chr1:169680905..169681683,2	K562	blood:
16	chr1:169690602..169692363-chr1:169698364..169700562,2	K562	blood:
17	chr1:169685122..169687361-chr1:169776503..169779359,2	MCF-7	breast:
18	chr1:169669179..169671320-chr1:169675894..169677671,2	K562	blood:
19	chr1:169691852..169693353-chr1:169762366..169764451,2	MCF-7	breast:
20	chr1:169609016..169611168-chr1:169613223..169616502,3	K562	blood:
21	chr1:169642958..169645181-chr1:169646382..169648638,2	MCF-7	breast:
22	chr1:169555471..169556167-chr1:169663467..169664121,3	MCF-7	breast:
23	chr1:169614149..169617850-chr1:169618797..169622086,4	K562	blood:
24	chr1:169642958..169645181-chr1:169646382..169648638,2	MCF-7	breast:
25	chr1:11969652..11970323-chr1:169649705..169650685,3	MCF-7	breast:
26	chr1:169658516..169660936-chr1:169662078..169664299,2	K562	blood:
27	chr1:169707608..169709249-chr1:169711620..169714505,2	MCF-7	breast:
28	chr1:169709712..169712944-chr1:169715789..169719606,5	MCF-7	breast:
29	chr1:169704931..169706505-chr1:169859799..169862220,2	K562	blood:
30	chr1:169658516..169660936-chr1:169662078..169664299,2	K562	blood:
31	chr1:169663115..169663861-chr1:169679931..169680901,2	MCF-7	breast:
32	chr1:169674141..169677050-chr1:169763005..169764633,2	MCF-7	breast:
33	chr1:169554938..169555875-chr1:169680931..169681496,2	MCF-7	breast:
34	chr1:169555259..169556175-chr1:169680918..169681805,3	MCF-7	breast:
35	chr1:169695880..169697994-chr1:169699455..169701036,2	MCF-7	breast:
36	chr1:169519013..169520404-chr1:169662765..169663989,4	MCF-7	breast:
37	chr1:169609016..169611168-chr1:169613223..169616502,3	K562	blood:
38	chr1:169570098..169571225-chr1:169663167..169664353,5	MCF-7	breast:
39	chr1:169697490..169699500-chr1:169702198..169704978,2	MCF-7	breast:
40	chr1:169519444..169520200-chr1:169680897..169681795,4	MCF-7	breast:
41	chr1:169668678..169669639-chr1:169778642..169779434,3	MCF-7	breast:
42	chr1:169668675..169669722-chr1:169778297..169779287,4	MCF-7	breast:
43	chr1:169614149..169618118-chr1:169618692..169623523,5	K562	blood:
44	chr1:169691841..169694549-chr1:169702477..169705562,3	MCF-7	breast:
45	chr1:169690602..169692363-chr1:169698364..169700562,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SELE-1	chr1:169660822-169660943	NONHSAT007471
2	lnc-SELE-1	chr1:169672396-169672470	NONHSAT007471
3	lnc-SELE-1	chr1:169665676-169665694	NONHSAT007471

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SELE	hsa-miR-31-5p	chr1:169693565-169693584

Variant related genes	Relation type
SELE	TF binding region
SELP	TF binding region
SELL	TF binding region
C1orf112	TF binding region
SELE	CpG island
SELP	CpG island
SELL	CpG island
C1orf112	CpG island
ENSG00000201801	chromatin interactions
ENSG00000000460	chromatin interactions
ENSG00000007908	chromatin interactions
ENSG00000198734	chromatin interactions
ENSG00000171806	chromatin interactions
ENSG00000188404	chromatin interactions

Extended variants
information (count: 4891 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:4891 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191193124	chr1:169593283-169593284	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs532445828	chr1:169593383-169593384	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs547529255	chr1:169593400-169593401	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs183743562	chr1:169593409-169593410	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs530005435	chr1:169593478-169593479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548569665	chr1:169593501-169593502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377114437	chr1:169593519-169593520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141768304	chr1:169593550-169593551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538160932	chr1:169593636-169593637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs3917861	chr1:169593680-169593681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9787264	chr1:169593701-169593702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138402137	chr1:169593712-169593713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188498199	chr1:169593734-169593735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs3917671	chr1:169593736-169593737	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs572109524	chr1:169593786-169593787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143235489	chr1:169593871-169593872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554564610	chr1:169593873-169593874	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576643702	chr1:169593874-169593875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543733037	chr1:169593892-169593893	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192793325	chr1:169593902-169593903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577060613	chr1:169593930-169593931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148306037	chr1:169593945-169593946	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559376545	chr1:169593987-169593988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528702447	chr1:169593989-169593990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3917670	chr1:169594010-169594011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541825985	chr1:169594040-169594041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563736787	chr1:169594062-169594063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531486835	chr1:169594145-169594146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141330882	chr1:169594194-169594195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571458721	chr1:169594220-169594221	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs77786712	chr1:169594227-169594228	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs547634614	chr1:169594239-169594240	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs565603398	chr1:169594302-169594303	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs536380285	chr1:169594306-169594307	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs184889557	chr1:169594333-169594334	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs569678219	chr1:169594354-169594355	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs546855714	chr1:169594538-169594539	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs537336006	chr1:169594542-169594543	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs150801730	chr1:169594562-169594563	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs561436561	chr1:169594619-169594620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577125867	chr1:169594662-169594663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530007959	chr1:169594669-169594670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6660207	chr1:169594692-169594693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551247332	chr1:169594740-169594741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553548058	chr1:169594757-169594758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs139273114	chr1:169594758-169594759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542338970	chr1:169594769-169594770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10919199	chr1:169594837-169594838	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182050821	chr1:169594975-169594976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184808816	chr1:169594997-169594998	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169585200-169593400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr1:169590600-169593600	Enhancers	Dnd41	blood
3	chr1:169590800-169595200	Weak transcription	Lung	lung
4	chr1:169591600-169599600	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr1:169592200-169594200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:169592200-169594600	Enhancers	HUVEC	blood vessel
7	chr1:169592200-169594800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr1:169592200-169595600	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr1:169592200-169597600	Enhancers	Primary T cells from cord blood	blood
10	chr1:169592200-169598400	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr1:169592200-169599400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr1:169592200-169599600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr1:169592200-169599800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr1:169592400-169593600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr1:169592400-169595000	Enhancers	Fetal Thymus	thymus
16	chr1:169592400-169596000	Enhancers	Primary T cells fromperipheralblood	blood
17	chr1:169592600-169593600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:169592600-169594200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr1:169592600-169595000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr1:169592800-169594200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:169593200-169593800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr1:169593200-169594000	Weak transcription	Thymus	Thymus
23	chr1:169593400-169594800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr1:169593600-169594400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr1:169593600-169596200	Enhancers	Primary hematopoietic stem cells	blood
26	chr1:169593600-169597000	Weak transcription	Dnd41	blood
27	chr1:169593800-169594600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr1:169593800-169596000	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr1:169594000-169594200	Enhancers	Thymus	Thymus
30	chr1:169594000-169594800	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr1:169594000-169595800	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr1:169594200-169594400	Weak transcription	Thymus	Thymus
33	chr1:169594200-169594600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr1:169594200-169597200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr1:169594200-169597400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr1:169594400-169594800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr1:169594400-169599400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:169594600-169597400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:169594600-169599000	Weak transcription	HUVEC	blood vessel
40	chr1:169594800-169596200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr1:169594800-169597200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr1:169594800-169597800	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr1:169595000-169595400	Weak transcription	Fetal Thymus	thymus
44	chr1:169595000-169597200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr1:169595400-169595600	Enhancers	Fetal Thymus	thymus
46	chr1:169595600-169596800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr1:169595600-169597200	Weak transcription	Fetal Thymus	thymus
48	chr1:169595800-169597600	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr1:169596000-169597000	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr1:169596000-169597400	Weak transcription	Primary monocytes fromperipheralblood	blood

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