Variant report

Variant	nsv872541
Chromosome Location	chr1:169672360-169695815
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	chr1:169680921-169681465	HepG2	liver:	n/a	n/a
2	BCLAF1	chr1:169680636-169681479	GM12878	blood:	n/a	n/a
3	BHLHE40	chr1:169681194-169681394	K562	blood:	n/a	n/a
4	CEBPB	chr1:169695377-169695730	HCT-116	colon:	n/a	n/a
5	CEBPB	chr1:169695487-169695688	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:169695414-169695763	K562	blood:	n/a	n/a
7	CEBPB	chr1:169695481-169695743	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:169695408-169695720	A549	lung:	n/a	n/a
9	CEBPB	chr1:169695403-169695746	K562	blood:	n/a	n/a
10	CEBPB	chr1:169695403-169695719	MCF-7	breast:	n/a	n/a
11	CHD1	chr1:169680684-169681360	GM12878	blood:	n/a	n/a
12	CHD2	chr1:169680659-169681482	GM12878	blood:	n/a	n/a
13	CTCF	chr1:169680796-169680955	NHEK	skin:	n/a	n/a
14	CTCF	chr1:169680760-169680910	GM12871	blood:	n/a	n/a
15	CTCF	chr1:169680827-169680994	K562	blood:	n/a	n/a
16	CTCF	chr1:169680760-169680910	NHEK	skin:	n/a	n/a
17	CTCF	chr1:169681240-169681390	WI-38	lung:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
18	CTCF	chr1:169681280-169681430	GM12873	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
19	CTCF	chr1:169681300-169681450	GM12869	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
20	CTCF	chr1:169695500-169695650	HCFaa	heart:	n/a	n/a
21	CTCF	chr1:169681148-169681426	A549	lung:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
22	CTCF	chr1:169681235-169681472	MCF-7	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
23	CTCF	chr1:169681231-169681489	ProgFib	skin:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
24	CTCF	chr1:169680800-169680950	GM12865	blood:	n/a	n/a
25	CTCF	chr1:169680804-169681019	GM13977	blood:	n/a	n/a
26	CTCF	chr1:169681228-169681501	GM10248	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
27	CTCF	chr1:169680700-169680850	BJ	skin:	n/a	n/a
28	CTCF	chr1:169681300-169681450	HFF-Myc	foreskin:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
29	CTCF	chr1:169681166-169681475	HepG2	liver:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
30	CTCF	chr1:169680880-169681030	Caco-2	colon:	n/a	n/a
31	CTCF	chr1:169680860-169681010	GM06990	blood:	n/a	n/a
32	CTCF	chr1:169681240-169681390	NHDF-neo	bronchial:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
33	CTCF	chr1:169681122-169681569	T-47D	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
34	CTCF	chr1:169680840-169680990	HPF	lung:	n/a	n/a
35	CTCF	chr1:169695400-169695550	HCT-116	colon:	n/a	n/a
36	CTCF	chr1:169680820-169680970	GM12868	blood:	n/a	n/a
37	CTCF	chr1:169680844-169680952	GM20000	blood:	n/a	n/a
38	CTCF	chr1:169681098-169681503	A549	lung:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
39	CTCF	chr1:169681204-169681496	Hela-S3	cervix:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
40	CTCF	chr1:169695540-169695690	HCT-116	colon:	n/a	n/a
41	CTCF	chr1:169680792-169680953	Gliobla	brain:	n/a	n/a
42	CTCF	chr1:169681260-169681410	GM12801	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
43	CTCF	chr1:169681260-169681410	GM12870	blood:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
44	CTCF	chr1:169680800-169680950	HCFaa	heart:	n/a	n/a
45	CTCF	chr1:169681260-169681410	HMF	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
46	CTCF	chr1:169681280-169681430	AoAF	blood vessel:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
47	CTCF	chr1:169681300-169681450	MCF-7	breast:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
48	CTCF	chr1:169680740-169680890	GM12864	blood:	n/a	n/a
49	CTCF	chr1:169681260-169681410	HEK293	kidney:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360
50	CTCF	chr1:169680643-169681596	SK-N-SH	brain:	n/a	chr1:169681351-169681358 chr1:169681344-169681362 chr1:169681339-169681360

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169693534-169693584	AG09309	skin:	n/a
2	chr1:169680613-169680663	RPTEC	kidney:	n/a
3	chr1:169679199-169679249	GM06990	blood:	n/a
4	chr1:169681333-169681383	PrEC	prostate:	n/a
5	chr1:169681333-169681383	HRE	kidney:	n/a
6	chr1:169681427-169681477	HUVEC	blood vessel:	n/a
7	chr1:169681333-169681383	ECC-1	luminal epithelium:	n/a
8	chr1:169681427-169681477	Hela-S3	cervix:	n/a
9	chr1:169681333-169681383	HIPEpiC	eye:	n/a
10	chr1:169681427-169681477	ovcar-3	ovarian:	n/a
11	chr1:169681427-169681477	RPTEC	kidney:	n/a
12	chr1:169679199-169679249	HUVEC	blood vessel:	n/a
13	chr1:169679199-169679249	GM12878	blood:	n/a
14	chr1:169679199-169679249	MCF10A-Er-Src	breast:	n/a
15	chr1:169681427-169681477	T-47D	breast:	n/a
16	chr1:169680613-169680663	HEK293	kidney:	embryo
17	chr1:169679199-169679249	HCF	heart:	n/a
18	chr1:169681333-169681383	HEEpiC	esophagus:	n/a
19	chr1:169693534-169693584	SK-N-MC	brain:	n/a
20	chr1:169679199-169679249	AoSMC	blood vessel:	n/a
21	chr1:169681427-169681477	NB4	blood:	n/a
22	chr1:169681333-169681383	HEK293	kidney:	embryo
23	chr1:169693534-169693584	HCPEpiC	choroid plexus:	n/a
24	chr1:169681333-169681383	GM06990	blood:	n/a
25	chr1:169693534-169693584	HMEC	breast:	n/a
26	chr1:169679199-169679249	NT2-D1	testis:	n/a
27	chr1:169693534-169693584	GM19239	blood:	n/a
28	chr1:169680613-169680663	AoSMC	blood vessel:	n/a
29	chr1:169693534-169693584	Jurkat	blood:	n/a
30	chr1:169679199-169679249	AG10803	skin:	n/a
31	chr1:169679199-169679249	MCF-7	breast:	n/a
32	chr1:169680613-169680663	Hela-S3	cervix:	n/a
33	chr1:169681427-169681477	NHBE	bronchial:	n/a
34	chr1:169681427-169681477	AG09309	skin:	n/a
35	chr1:169680613-169680663	GM06990	blood:	n/a
36	chr1:169680613-169680663	HUVEC	blood vessel:	n/a
37	chr1:169680613-169680663	AG04449	skin:	fetal
38	chr1:169679199-169679249	SK-N-SH_RA	brain:	n/a
39	chr1:169680613-169680663	MCF-7	breast:	n/a
40	chr1:169680613-169680663	GM12878	blood:	n/a
41	chr1:169680613-169680663	HRE	kidney:	n/a
42	chr1:169680613-169680663	HL-60	blood:	n/a
43	chr1:169693534-169693584	HL-60	blood:	n/a
44	chr1:169681333-169681383	Jurkat	blood:	n/a
45	chr1:169679199-169679249	CMK	blood:	n/a
46	chr1:169681427-169681477	AG04449	skin:	fetal
47	chr1:169681427-169681477	BE2_C	brain:	n/a
48	chr1:169693534-169693584	HRPEpiC	eye:	n/a
49	chr1:169693534-169693584	HUVEC	blood vessel:	n/a
50	chr1:169693534-169693584	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:169679878..169683283-chr1:169762041..169765464,5	MCF-7	breast:
2	chr1:169690602..169692363-chr1:169698364..169700562,2	K562	blood:
3	chr1:169519444..169520200-chr1:169680897..169681795,4	MCF-7	breast:
4	chr1:169691841..169694549-chr1:169702477..169705562,3	MCF-7	breast:
5	chr1:168572840..168573443-chr1:169680986..169681557,2	MCF-7	breast:
6	chr1:168572487..168573340-chr1:169680905..169681683,2	K562	blood:
7	chr1:169569836..169571238-chr1:169680901..169681521,6	MCF-7	breast:
8	chr1:169555259..169556175-chr1:169680918..169681805,3	MCF-7	breast:
9	chr1:169691852..169693353-chr1:169762366..169764451,2	MCF-7	breast:
10	chr1:169680922..169681530-chr1:169748582..169749325,2	MCF-7	breast:
11	chr1:169674141..169677050-chr1:169763005..169764633,2	MCF-7	breast:
12	chr1:169680417..169682445-chr1:169762164..169765185,3	MCF-7	breast:
13	chr1:169554938..169555875-chr1:169680931..169681496,2	MCF-7	breast:
14	chr1:169685122..169687361-chr1:169776503..169779359,2	MCF-7	breast:
15	chr1:169669179..169671320-chr1:169675894..169677671,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SELE-1	chr1:169672396-169672470	NONHSAT007471

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

Variant related genes	Relation type
SELL	TF binding region
SELL	CpG island
ENSG00000007908	chromatin interactions
ENSG00000000460	chromatin interactions
ENSG00000171806	chromatin interactions
ENSG00000198734	chromatin interactions

Extended variants
information (count: 1026 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1026 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4987313	chr1:169672360-169672361	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184513878	chr1:169672361-169672362	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147585835	chr1:169672393-169672394	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561566828	chr1:169672413-169672414	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs574888692	chr1:169672427-169672428	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs188911090	chr1:169672463-169672464	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs550385079	chr1:169672485-169672486	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182540776	chr1:169672508-169672509	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs137853581	chr1:169672555-169672556	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532610601	chr1:169672594-169672595	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544690924	chr1:169672595-169672596	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs202128116	chr1:169672596-169672597	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566025367	chr1:169672609-169672610	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530579683	chr1:169672612-169672613	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533840923	chr1:169672638-169672639	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76237714	chr1:169672641-169672642	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567213811	chr1:169672682-169672683	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187113161	chr1:169672785-169672786	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191120285	chr1:169672786-169672787	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73039456	chr1:169672796-169672797	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs12137905	chr1:169672867-169672868	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs553496190	chr1:169672873-169672874	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12087033	chr1:169672898-169672899	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs180741180	chr1:169672899-169672900	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35535713	chr1:169672977-169672978	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12072966	chr1:169672990-169672991	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs12087116	chr1:169673032-169673033	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532023623	chr1:169673051-169673052	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs185739372	chr1:169673053-169673054	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35383673	chr1:169673063-169673064	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565443738	chr1:169673131-169673132	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151151923	chr1:169673140-169673141	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200878814	chr1:169673156-169673157	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527384791	chr1:169673157-169673158	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547823807	chr1:169673237-169673238	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4987312	chr1:169673262-169673263	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528120129	chr1:169673395-169673396	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566766859	chr1:169673411-169673412	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114228238	chr1:169673460-169673461	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141079547	chr1:169673465-169673466	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537719996	chr1:169673472-169673473	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556100719	chr1:169673473-169673474	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571378773	chr1:169673481-169673482	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145174074	chr1:169673493-169673494	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553874344	chr1:169673508-169673509	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572157318	chr1:169673527-169673528	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4987311	chr1:169673545-169673546	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397843678	chr1:169673551-169673552	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536282501	chr1:169673557-169673558	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554577508	chr1:169673570-169673571	Genic enhancers Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169662400-169676000	Genic enhancers	Primary B cells from peripheral blood	blood
2	chr1:169663200-169674000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr1:169664000-169673400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:169664000-169674000	Genic enhancers	Fetal Thymus	thymus
5	chr1:169664000-169674200	Genic enhancers	Primary T cells fromperipheralblood	blood
6	chr1:169666200-169673800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
7	chr1:169667600-169673600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
8	chr1:169667600-169676800	Genic enhancers	Primary monocytes fromperipheralblood	blood
9	chr1:169668000-169677400	Transcr. at gene 5' and 3'	Primary T cells from cord blood	blood
10	chr1:169669400-169673000	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr1:169669600-169672800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr1:169669600-169674400	Genic enhancers	Primary hematopoietic stem cells	blood
13	chr1:169670000-169673600	Weak transcription	GM12878-XiMat	blood
14	chr1:169670200-169673200	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr1:169670600-169678000	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
16	chr1:169670800-169672800	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
17	chr1:169671000-169672600	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr1:169671000-169673600	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr1:169671000-169675000	Genic enhancers	Monocytes-CD14+_RO01746	blood
20	chr1:169671200-169673600	Genic enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr1:169671200-169679400	Transcr. at gene 5' and 3'	Dnd41	blood
22	chr1:169671400-169673200	Genic enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr1:169671600-169673400	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr1:169671800-169673600	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr1:169672000-169672600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:169672000-169672800	Weak transcription	Thymus	Thymus
27	chr1:169672000-169672800	Strong transcription	Spleen	Spleen
28	chr1:169672000-169673200	Genic enhancers	Primary B cells from cord blood	blood
29	chr1:169672200-169672800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr1:169672600-169677400	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
31	chr1:169672600-169678000	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:169672800-169673000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr1:169672800-169673200	Enhancers	Thymus	Thymus
34	chr1:169672800-169673400	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr1:169672800-169674600	Weak transcription	Spleen	Spleen
36	chr1:169672800-169676000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr1:169673000-169673400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr1:169673000-169673600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr1:169673200-169673400	Weak transcription	Thymus	Thymus
40	chr1:169673200-169674600	Transcr. at gene 5' and 3'	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr1:169673200-169676800	Transcr. at gene 5' and 3'	Primary T helper naive cells from peripheral blood	blood
42	chr1:169673200-169678400	Transcr. at gene 5' and 3'	Primary B cells from cord blood	blood
43	chr1:169673400-169673600	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:169673400-169673800	Transcr. at gene 5' and 3'	Primary T helper memory cells from peripheral blood 1	blood
45	chr1:169673400-169674000	Enhancers	Thymus	Thymus
46	chr1:169673400-169674400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:169673400-169676600	Transcr. at gene 5' and 3'	Primary T helper naive cells fromperipheralblood	blood
48	chr1:169673600-169674000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
49	chr1:169673600-169674000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr1:169673600-169674000	Transcr. at gene 5' and 3'	Primary T killer memory cells from peripheral blood	blood

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