Variant report

Variant	esv3384628
Chromosome Location	chr1:153893928-153896576
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:833)
CpG islands
(count:859)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:153895552-153895878	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:153895475-153896162	K562	blood:	n/a	n/a
3	ARID3A	chr1:153894525-153894675	HepG2	liver:	n/a	n/a
4	ATF1	chr1:153895430-153895788	K562	blood:	n/a	n/a
5	ATF2	chr1:153895505-153896208	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr1:153895430-153896376	GM12878	blood:	n/a	n/a
7	ATF2	chr1:153895530-153896284	GM12878	blood:	n/a	n/a
8	ATF2	chr1:153895496-153896129	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr1:153895561-153896100	A549	lung:	n/a	n/a
10	BACH1	chr1:153895679-153896291	K562	blood:	n/a	n/a
11	BACH1	chr1:153895465-153896537	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr1:153895488-153896193	A549	lung:	n/a	chr1:153895828-153895837
13	BCL3	chr1:153895472-153896312	A549	lung:	n/a	chr1:153895828-153895837
14	BCLAF1	chr1:153895524-153896181	GM12878	blood:	n/a	chr1:153895828-153895837
15	BCLAF1	chr1:153895432-153896352	GM12878	blood:	n/a	chr1:153895828-153895837
16	BHLHE40	chr1:153895088-153895191	K562	blood:	n/a	n/a
17	BHLHE40	chr1:153895520-153896225	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:153895530-153896398	K562	blood:	n/a	n/a
19	BHLHE40	chr1:153895094-153895240	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:153894255-153894750	K562	blood:	n/a	n/a
21	BRCA1	chr1:153895134-153896731	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr1:153895560-153896100	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr1:153895801-153896090	HepG2	liver:	n/a	n/a
24	BRCA1	chr1:153894185-153894302	GM12878	blood:	n/a	n/a
25	BRCA1	chr1:153895503-153896151	GM12878	blood:	n/a	n/a
26	CBX3	chr1:153895005-153896297	K562	blood:	n/a	n/a
27	CCNT2	chr1:153894520-153896218	K562	blood:	n/a	chr1:153895326-153895335 chr1:153895016-153895025
28	CEBPB	chr1:153896428-153896696	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:153895648-153895997	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:153895700-153896024	GM12878	blood:	n/a	n/a
31	CEBPB	chr1:153895482-153896377	GM12878	blood:	n/a	n/a
32	CEBPB	chr1:153895502-153896000	Hela-S3	cervix:	n/a	n/a
33	CEBPD	chr1:153895466-153895947	HepG2	liver:	n/a	n/a
34	CEBPZ	chr1:153895426-153895774	HepG2	liver:	n/a	n/a
35	CHD1	chr1:153895629-153896633	GM12878	blood:	n/a	n/a
36	CHD1	chr1:153894423-153894703	GM12878	blood:	n/a	n/a
37	CHD1	chr1:153895786-153896117	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr1:153894942-153896410	GM12878	blood:	n/a	chr1:153895015-153895025
39	CHD2	chr1:153894567-153896341	Hela-S3	cervix:	n/a	chr1:153895015-153895025
40	CHD2	chr1:153894963-153896212	HepG2	liver:	n/a	chr1:153895015-153895025
41	CHD2	chr1:153894813-153896236	K562	blood:	n/a	chr1:153895015-153895025
42	CHD2	chr1:153894987-153896377	H1-hESC	embryonic stem cell:	n/a	chr1:153895015-153895025
43	CREB1	chr1:153895205-153896001	A549	lung:	n/a	n/a
44	CREB1	chr1:153895246-153895827	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr1:153894885-153895998	GM12878	blood:	n/a	n/a
46	CREB1	chr1:153895410-153895822	A549	lung:	n/a	n/a
47	CTCF	chr1:153895080-153895230	HFF	foreskin:	n/a	n/a
48	CTCF	chr1:153895180-153895330	AG04450	lung:	n/a	n/a
49	CTCF	chr1:153895140-153895290	GM12865	blood:	n/a	n/a
50	CTCF	chr1:153895140-153895290	GM12878	blood:	n/a	n/a

(count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153894941-153894991	HCT-116	colon:	n/a
2	chr1:153895881-153895931	IMR90	lung:	fetal
3	chr1:153895885-153895935	Jurkat	blood:	n/a
4	chr1:153895398-153895448	NB4	blood:	n/a
5	chr1:153895721-153895771	AG10803	skin:	n/a
6	chr1:153894941-153894991	HCT-116	colon:	n/a
7	chr1:153895881-153895931	IMR90	lung:	fetal
8	chr1:153895885-153895935	Jurkat	blood:	n/a
9	chr1:153895398-153895448	NB4	blood:	n/a
10	chr1:153895721-153895771	AG10803	skin:	n/a
11	chr1:153895881-153895931	ECC-1	luminal epithelium:	n/a
12	chr1:153895885-153895935	SAEC	small airway:	n/a
13	chr1:153895721-153895771	Hela-S3	cervix:	n/a
14	chr1:153895888-153895938	SK-N-MC	brain:	n/a
15	chr1:153895885-153895935	BE2_C	brain:	n/a
16	chr1:153895961-153896011	HMEC	breast:	n/a
17	chr1:153895885-153895935	AoSMC	blood vessel:	n/a
18	chr1:153895324-153895374	HAEpiC	amniotic membrane:	n/a
19	chr1:153895324-153895374	HCM	heart:	n/a
20	chr1:153895177-153895227	AG09309	skin:	n/a
21	chr1:153895177-153895227	A549	lung:	n/a
22	chr1:153894579-153894629	AoSMC	blood vessel:	n/a
23	chr1:153894579-153894629	AG04450	lung:	fetal
24	chr1:153895546-153895596	AG04450	lung:	fetal
25	chr1:153895885-153895935	GM12892	blood:	n/a
26	chr1:153895888-153895938	RPTEC	kidney:	n/a
27	chr1:153895448-153895498	AoSMC	blood vessel:	n/a
28	chr1:153895881-153895931	PrEC	prostate:	n/a
29	chr1:153894579-153894629	HEK293	kidney:	embryo
30	chr1:153895888-153895938	ProgFib	skin:	n/a
31	chr1:153894579-153894629	A549	lung:	n/a
32	chr1:153894579-153894629	HMEC	breast:	n/a
33	chr1:153895721-153895771	HMEC	breast:	n/a
34	chr1:153895888-153895938	HNPCEpiC	eye:	n/a
35	chr1:153895721-153895771	GM12891	blood:	n/a
36	chr1:153895607-153895657	NHBE	bronchial:	n/a
37	chr1:153895961-153896011	U87	brain:	n/a
38	chr1:153895888-153895938	HepG2	liver:	n/a
39	chr1:153895177-153895227	HUVEC	blood vessel:	n/a
40	chr1:153895448-153895498	A549	lung:	n/a
41	chr1:153895888-153895938	HRE	kidney:	n/a
42	chr1:153895177-153895227	Hepatocyte	liver:	n/a
43	chr1:153895546-153895596	GM12878	blood:	n/a
44	chr1:153895885-153895935	T-47D	breast:	n/a
45	chr1:153895448-153895498	HepG2	liver:	n/a
46	chr1:153895324-153895374	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:153894941-153894991	HRE	kidney:	n/a
48	chr1:153895885-153895935	CMK	blood:	n/a
49	chr1:153895721-153895771	AG04449	skin:	fetal
50	chr1:153895398-153895448	ECC-1	luminal epithelium:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153890756..153897034-chr1:153961597..153964863,14	K562	blood:
2	chr1:153895897..153896422-chr11:48153597..48154395,2	Hela-S3	cervix:
3	chr1:153895740..153897837-chr1:153943889..153946468,2	K562	blood:
4	chr1:153642898..153644985-chr1:153891363..153894144,2	K562	blood:
5	chr1:153895003..153895633-chr10:70166494..70167290,2	Hela-S3	cervix:
6	chr1:153894942..153895704-chr1:153918773..153919666,3	K562	blood:
7	chr1:153895633..153896175-chr1:153949945..153950661,2	Hela-S3	cervix:
8	chr1:153877108..153878682-chr1:153895765..153897266,2	MCF-7	breast:
9	chr1:153813066..153815919-chr1:153892208..153893963,2	MCF-7	breast:
10	chr1:153858733..153861625-chr1:153893307..153895024,2	K562	blood:
11	chr1:153892719..153895039-chr1:153953793..153956278,2	K562	blood:
12	chr1:153893510..153896669-chr1:153958441..153960611,3	K562	blood:
13	chr1:153792897..153795866-chr1:153896474..153898654,2	MCF-7	breast:
14	chr1:153883515..153885221-chr1:153892964..153894776,3	MCF-7	breast:
15	chr1:153759800..153761704-chr1:153893842..153895431,2	K562	blood:
16	chr1:153774428..153778178-chr1:153892159..153894443,3	MCF-7	breast:
17	chr1:153746879..153748867-chr1:153894033..153896594,2	K562	blood:
18	chr1:153699430..153701547-chr1:153893565..153895608,2	MCF-7	breast:
19	chr1:153892664..153896587-chr1:153948190..153951187,6	K562	blood:
20	chr1:153858652..153861331-chr1:153892093..153894371,2	MCF-7	breast:
21	chr1:153754212..153755933-chr1:153895678..153897558,2	MCF-7	breast:
22	chr1:153537683..153540046-chr1:153895076..153896651,2	K562	blood:
23	chr1:153747665..153750002-chr1:153895693..153897209,2	MCF-7	breast:
24	chr1:153876373..153878542-chr1:153895885..153898675,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CREB3L4-1	chr1:153895762-153896438	NONHSAT006552

No data

Variant related genes	Relation type
GATAD2B	TF binding region
GATAD2B	CpG island
ENSG00000143621	chromatin interactions
ENSG00000177954	chromatin interactions
ENSG00000198837	chromatin interactions
ENSG00000143624	chromatin interactions
ENSG00000143543	chromatin interactions
ENSG00000143554	chromatin interactions
ENSG00000204130	chromatin interactions
ENSG00000272654	chromatin interactions
ENSG00000143545	chromatin interactions
ENSG00000196754	chromatin interactions

Extended variants
information (count: 89 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78542912	chr1:153893962-153893963	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs35948383	chr1:153893999-153894000	Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs545987145	chr1:153894007-153894008	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs558107004	chr1:153894022-153894023	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs576359029	chr1:153894053-153894054	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs547914968	chr1:153894054-153894055	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs199804315	chr1:153894073-153894074	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs567410624	chr1:153894077-153894078	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs375613490	chr1:153894083-153894084	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs12070549	chr1:153894084-153894085	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs543845756	chr1:153894086-153894087	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs561980674	chr1:153894094-153894095	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs189896410	chr1:153894097-153894098	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs529285502	chr1:153894161-153894162	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs541194178	chr1:153894232-153894233	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs76809384	chr1:153894262-153894263	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs533361480	chr1:153894269-153894270	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs76879978	chr1:153894277-153894278	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs369587263	chr1:153894306-153894307	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs531152147	chr1:153894332-153894333	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs563585334	chr1:153894343-153894344	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs182170131	chr1:153894404-153894405	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs535415134	chr1:153894439-153894440	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs1416843	chr1:153894447-153894448	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs572684642	chr1:153894484-153894485	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs34438060	chr1:153894495-153894496	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs541698763	chr1:153894517-153894518	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs553602363	chr1:153894603-153894604	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs565741605	chr1:153894604-153894605	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs539649462	chr1:153894623-153894624	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs148732990	chr1:153894665-153894666	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs576293210	chr1:153894686-153894687	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs372072815	chr1:153894693-153894694	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs142336459	chr1:153894711-153894712	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs570451535	chr1:153894764-153894765	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs529245593	chr1:153894775-153894776	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs151287239	chr1:153894821-153894822	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs573982684	chr1:153894828-153894829	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs541378618	chr1:153894930-153894931	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs559611914	chr1:153894958-153894959	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs533205400	chr1:153895198-153895199	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs545091403	chr1:153895223-153895224	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs563588960	chr1:153895305-153895306	Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs530990577	chr1:153895516-153895517	Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs140541322	chr1:153895547-153895548	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs576737972	chr1:153895550-153895551	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs111228526	chr1:153895581-153895582	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs147097629	chr1:153895628-153895629	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs537442262	chr1:153895654-153895655	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs528904703	chr1:153895662-153895663	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	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
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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	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
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Liver carcinoma	19366792	CNVD
Neuroblastoma	18923191	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	chr1:153846200-153894200	Weak transcription	Esophagus	oesophagus
2	chr1:153866400-153894000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr1:153878600-153894000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:153891400-153894000	Enhancers	Colon Smooth Muscle	Colon
5	chr1:153891600-153894800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:153891800-153894000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr1:153891800-153894000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
8	chr1:153891800-153894000	Enhancers	Stomach Mucosa	stomach
9	chr1:153891800-153894400	Flanking Active TSS	Fetal Brain Female	brain
10	chr1:153892200-153894000	Enhancers	Pancreas	Pancrea
11	chr1:153892200-153894000	Enhancers	Psoas Muscle	Psoas
12	chr1:153892200-153894600	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr1:153892400-153894000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:153892400-153894000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr1:153892400-153894000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr1:153892400-153894000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:153892400-153894000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr1:153892400-153894000	Enhancers	Gastric	stomach
19	chr1:153892400-153894200	Enhancers	Placenta	Placenta
20	chr1:153892400-153894200	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr1:153892400-153894400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:153892400-153894400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:153892400-153894400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr1:153892400-153894400	Flanking Active TSS	Brain Angular Gyrus	brain
25	chr1:153892400-153894400	Flanking Active TSS	Brain Germinal Matrix	brain
26	chr1:153892400-153894400	Enhancers	Spleen	Spleen
27	chr1:153892400-153894600	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr1:153892400-153894600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
29	chr1:153892400-153894600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:153892400-153894600	Transcr. at gene 5' and 3'	Dnd41	blood
31	chr1:153892400-153895000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:153892600-153894000	Enhancers	Left Ventricle	heart
33	chr1:153892600-153894000	Enhancers	HSMM	muscle
34	chr1:153892600-153894000	Flanking Active TSS	NHEK	skin
35	chr1:153892600-153894400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:153892600-153894400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr1:153892600-153894400	Flanking Active TSS	Brain Anterior Caudate	brain
38	chr1:153892600-153894400	Flanking Active TSS	Hela-S3	cervix
39	chr1:153892600-153894800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
40	chr1:153892600-153894800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr1:153892600-153894800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr1:153892800-153894000	Flanking Active TSS	HMEC	breast
43	chr1:153892800-153894200	Enhancers	Primary B cells from peripheral blood	blood
44	chr1:153892800-153894400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr1:153892800-153894400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
46	chr1:153892800-153894600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr1:153892800-153894600	Flanking Active TSS	Brain Cingulate Gyrus	brain
48	chr1:153892800-153894600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr1:153892800-153894800	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr1:153893000-153894000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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