Variant report

Variant	nsv946417
Chromosome Location	chr1:155529941-155533143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:695)
CpG islands
(count:612)
Chromatin interactive
region (count:37)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:695 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155532749-155533151	K562	blood:	n/a	n/a
2	ATF2	chr1:155532596-155533085	GM12878	blood:	n/a	n/a
3	ATF2	chr1:155532606-155533273	GM12878	blood:	n/a	n/a
4	ATF3	chr1:155532730-155533195	A549	lung:	n/a	n/a
5	ATF3	chr1:155532408-155532643	K562	blood:	n/a	n/a
6	BACH1	chr1:155532759-155533072	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:155532778-155532882	K562	blood:	n/a	n/a
8	BATF	chr1:155532878-155533223	GM12878	blood:	n/a	n/a
9	BATF	chr1:155531493-155531877	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:155532829-155533461	GM12878	blood:	n/a	n/a
11	BCL11A	chr1:155531434-155531867	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:155532354-155532627	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:155531636-155531849	GM12878	blood:	n/a	n/a
14	BCL3	chr1:155532730-155533206	A549	lung:	n/a	n/a
15	BCL3	chr1:155532620-155533261	A549	lung:	n/a	n/a
16	BCLAF1	chr1:155532662-155533379	GM12878	blood:	n/a	n/a
17	BCLAF1	chr1:155532699-155533297	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:155532654-155533066	A549	lung:	n/a	n/a
19	BHLHE40	chr1:155532334-155533231	HepG2	liver:	n/a	n/a
20	BHLHE40	chr1:155532292-155533226	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:155532288-155533222	K562	blood:	n/a	n/a
22	BRCA1	chr1:155532796-155533205	HepG2	liver:	n/a	n/a
23	BRCA1	chr1:155532764-155533073	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr1:155532704-155533122	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr1:155532795-155533103	GM12878	blood:	n/a	n/a
26	CBX3	chr1:155531061-155531926	K562	blood:	n/a	n/a
27	CBX3	chr1:155532877-155533212	K562	blood:	n/a	n/a
28	CBX3	chr1:155532191-155534095	K562	blood:	n/a	n/a
29	CCNT2	chr1:155532298-155533256	K562	blood:	n/a	n/a
30	CEBPB	chr1:155532780-155533635	GM12878	blood:	n/a	n/a
31	CEBPD	chr1:155532087-155533267	K562	blood:	n/a	n/a
32	CEBPD	chr1:155532401-155533169	HepG2	liver:	n/a	n/a
33	CEBPD	chr1:155532932-155533171	HepG2	liver:	n/a	n/a
34	CEBPD	chr1:155532615-155533365	K562	blood:	n/a	n/a
35	CEBPD	chr1:155532576-155532784	HepG2	liver:	n/a	n/a
36	CHD1	chr1:155531752-155534107	IMR90	lung:	n/a	n/a
37	CHD1	chr1:155532026-155533406	GM12878	blood:	n/a	n/a
38	CHD1	chr1:155532695-155533205	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr1:155531928-155532001	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr1:155532438-155533220	HepG2	liver:	n/a	n/a
41	CHD2	chr1:155532871-155533071	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr1:155532413-155533215	K562	blood:	n/a	n/a
43	CHD2	chr1:155532368-155533219	GM12878	blood:	n/a	n/a
44	CHD2	chr1:155531842-155532139	GM12878	blood:	n/a	n/a
45	CHD2	chr1:155532293-155533147	Hela-S3	cervix:	n/a	n/a
46	CREB1	chr1:155532644-155532985	ECC-1	luminal epithelium:	n/a	n/a
47	CREB1	chr1:155532234-155533159	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr1:155532089-155533271	GM12878	blood:	n/a	n/a
49	CREB1	chr1:155532089-155533317	HepG2	liver:	n/a	n/a
50	CREB1	chr1:155532203-155533264	K562	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155532423-155532473	ECC-1	luminal epithelium:	n/a
2	chr1:155530669-155530719	NHDF-neo	bronchial:	n/a
3	chr1:155532423-155532473	ECC-1	luminal epithelium:	n/a
4	chr1:155530669-155530719	NHDF-neo	bronchial:	n/a
5	chr1:155533016-155533066	HNPCEpiC	eye:	n/a
6	chr1:155532420-155532470	HCM	heart:	n/a
7	chr1:155532420-155532470	HEK293	kidney:	embryo
8	chr1:155532423-155532473	AG04449	skin:	fetal
9	chr1:155532716-155532766	HCT-116	colon:	n/a
10	chr1:155530669-155530719	HIPEpiC	eye:	n/a
11	chr1:155532814-155532864	MCF10A-Er-Src	breast:	n/a
12	chr1:155530423-155530473	HRE	kidney:	n/a
13	chr1:155533016-155533066	BE2_C	brain:	n/a
14	chr1:155532716-155532766	SK-N-MC	brain:	n/a
15	chr1:155533016-155533066	NT2-D1	testis:	n/a
16	chr1:155532716-155532766	GM06990	blood:	n/a
17	chr1:155532722-155532772	SK-N-SH	brain:	n/a
18	chr1:155533016-155533066	NHDF-neo	bronchial:	n/a
19	chr1:155532814-155532864	GM19239	blood:	n/a
20	chr1:155530423-155530473	AG04449	skin:	fetal
21	chr1:155532420-155532470	AoSMC	blood vessel:	n/a
22	chr1:155533016-155533066	LNCaP	prostate:	n/a
23	chr1:155530669-155530719	NH-A	brain:	n/a
24	chr1:155532722-155532772	PrEC	prostate:	n/a
25	chr1:155533016-155533066	AG04449	skin:	fetal
26	chr1:155532420-155532470	NB4	blood:	n/a
27	chr1:155532814-155532864	HIPEpiC	eye:	n/a
28	chr1:155532722-155532772	ProgFib	skin:	n/a
29	chr1:155532814-155532864	Caco-2	colon:	n/a
30	chr1:155532814-155532864	IMR90	lung:	fetal
31	chr1:155532423-155532473	AoSMC	blood vessel:	n/a
32	chr1:155532420-155532470	GM06990	blood:	n/a
33	chr1:155532722-155532772	GM06990	blood:	n/a
34	chr1:155532423-155532473	SK-N-SH_RA	brain:	n/a
35	chr1:155530669-155530719	AG09309	skin:	n/a
36	chr1:155532548-155532598	K562	blood:	n/a
37	chr1:155532716-155532766	HRE	kidney:	n/a
38	chr1:155530423-155530473	A549	lung:	n/a
39	chr1:155530669-155530719	SAEC	small airway:	n/a
40	chr1:155532716-155532766	Hepatocyte	liver:	n/a
41	chr1:155532548-155532598	LNCaP	prostate:	n/a
42	chr1:155532722-155532772	NHBE	bronchial:	n/a
43	chr1:155532814-155532864	AG09309	skin:	n/a
44	chr1:155533016-155533066	SK-N-SH	brain:	n/a
45	chr1:155530669-155530719	ECC-1	luminal epithelium:	n/a
46	chr1:155532423-155532473	U87	brain:	n/a
47	chr1:155532716-155532766	PFSK-1	brain:	n/a
48	chr1:155533016-155533066	ECC-1	luminal epithelium:	n/a
49	chr1:155530423-155530473	HepG2	liver:	n/a
50	chr1:155532716-155532766	H1-hESC	embryonic stem cell:	embryo

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155532582..155533539-chr9:91926072..91926647,3	Hela-S3	cervix:
2	chr1:155532102..155532798-chr1:155657720..155658726,4	NB4	blood:
3	chr1:155292471..155294999-chr1:155531525..155533817,3	K562	blood:
4	chr1:155530812..155532531-chr1:155657028..155659724,4	K562	blood:
5	chr1:155532081..155532969-chr1:155658202..155658825,5	HCT-116	colon:
6	chr1:155291309..155295116-chr1:155530603..155535374,8	MCF-7	breast:
7	chr1:155532790..155533528-chr15:85291277..85292134,2	Hela-S3	cervix:
8	chr1:155520429..155523505-chr1:155527684..155531607,4	K562	blood:
9	chr1:155532881..155533454-chrX:47518051..47518637,2	Hela-S3	cervix:
10	chr1:155532724..155534552-chr1:155658209..155659716,2	K562	blood:
11	chr1:155499625..155501625-chr1:155533032..155534566,2	MCF-7	breast:
12	chr1:155163156..155164893-chr1:155532696..155534228,2	K562	blood:
13	chr1:155531168..155533264-chr1:155658199..155660031,3	MCF-7	breast:
14	chr1:155532088..155534231-chr8:145750623..145753092,2	MCF-7	breast:
15	chr1:155531963..155532590-chr12:56551850..56552623,2	Hela-S3	cervix:
16	chr1:155246581..155249773-chr1:155532192..155535114,5	MCF-7	breast:
17	chr1:155532819..155534394-chr1:155543476..155545822,2	K562	blood:
18	chr1:154934930..154937896-chr1:155531349..155532999,2	K562	blood:
19	chr1:155444626..155447232-chr1:155532733..155534954,2	MCF-7	breast:
20	chr1:155531220..155534536-chr1:155656727..155659727,4	MCF-7	breast:
21	chr1:155532716..155533474-chr19:571939..572844,2	Hela-S3	cervix:
22	chr1:155428479..155431081-chr1:155533087..155535825,2	K562	blood:
23	chr1:155530671..155532502-chr1:155535326..155537191,2	MCF-7	breast:
24	chr1:155532787..155533321-chr1:155658619..155659301,2	Hela-S3	cervix:
25	chr1:155532125..155532716-chr4:10117868..10118382,2	HCT-116	colon:
26	chr1:155532611..155533379-chr11:17229191..17230143,2	Hela-S3	cervix:
27	chr1:155292200..155295685-chr1:155531348..155534529,4	MCF-7	breast:
28	chr1:155256697..155258706-chr1:155531523..155534465,2	MCF-7	breast:
29	chr1:155533136..155533702-chr6:26031941..26032663,2	Hela-S3	cervix:
30	chr1:155532937..155533522-chr3:156544111..156544757,2	Hela-S3	cervix:
31	chr1:155533061..155533901-chr6:32939793..32940739,2	NB4	blood:
32	chr1:155292800..155294999-chr1:155531525..155533061,2	K562	blood:
33	chr1:155532088..155532960-chr1:155658209..155658720,2	MCF-7	breast:
34	chr1:155533054..155535636-chr1:155540451..155542741,3	MCF-7	breast:
35	chr1:155144807..155147212-chr1:155533013..155534550,2	K562	blood:
36	chr1:155532717..155533287-chr17:66508208..66509143,2	Hela-S3	cervix:
37	chr1:155241815..155243331-chr1:155532425..155534000,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MSTO1-1	chr1:155531821-155533775	ENSG00000235919.3
2	lnc-MSTO1-1	chr1:155531864-155532077	ENSG00000235919
3	lnc-MSTO1-1	chr1:155533041-155533735	ENSG00000235919
4	lnc-MSTO1-1	chr1:155532772-155533437	ENSG00000235919
5	lnc-MSTO1-1	chr1:155531772-155533735	NONHSAT006742
6	lnc-MSTO1-1	chr1:155531833-155532077	ENSG00000235919

No data

Variant related genes	Relation type
ASH1L-AS1	TF binding region
ASH1L	TF binding region
ASH1L-AS1	CpG island
ASH1L	CpG island
ENSG00000123975	chromatin interactions
ENSG00000267064	chromatin interactions
ENSG00000172270	chromatin interactions
ENSG00000163374	chromatin interactions
ENSG00000108946	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000257809	chromatin interactions
ENSG00000166716	chromatin interactions
ENSG00000267751	chromatin interactions
ENSG00000254402	chromatin interactions
ENSG00000197980	chromatin interactions
ENSG00000143630	chromatin interactions
ENSG00000163348	chromatin interactions
ENSG00000132676	chromatin interactions
ENSG00000163463	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000263756	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000070081	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000176444	chromatin interactions
ENSG00000092841	chromatin interactions
ENSG00000011405	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000126756	chromatin interactions
ENSG00000271267	chromatin interactions

Extended variants
information (count: 107 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:107 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114109825	chr1:155529962-155529963	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs185203269	chr1:155529987-155529988	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs6673172	chr1:155530012-155530013	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs189627428	chr1:155530033-155530034	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs147473764	chr1:155530054-155530055	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs539295161	chr1:155530193-155530194	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs115907380	chr1:155530203-155530204	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs112892897	chr1:155530224-155530225	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs182110818	chr1:155530239-155530240	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs556302589	chr1:155530301-155530302	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs577079618	chr1:155530333-155530334	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs186310399	chr1:155530393-155530394	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs534299012	chr1:155530411-155530412	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs57956370	chr1:155530415-155530416	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs570934987	chr1:155530424-155530425	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs556385578	chr1:155530429-155530430	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs538302316	chr1:155530445-155530446	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs556647596	chr1:155530446-155530447	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs569888596	chr1:155530503-155530504	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs543254183	chr1:155530551-155530552	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs554943416	chr1:155530563-155530564	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs518612	chr1:155530579-155530580	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs115462726	chr1:155530580-155530581	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs518584	chr1:155530590-155530591	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs565250513	chr1:155530593-155530594	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532553775	chr1:155530606-155530607	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs544675131	chr1:155530626-155530627	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs368866119	chr1:155530638-155530639	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs563036336	chr1:155530680-155530681	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs60564998	chr1:155530702-155530703	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs530613550	chr1:155530760-155530761	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs549186559	chr1:155530810-155530811	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs372532217	chr1:155530850-155530851	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs528344593	chr1:155530868-155530869	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs546496349	chr1:155530875-155530876	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs570872002	chr1:155530887-155530888	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs376821523	chr1:155530975-155530976	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs556635386	chr1:155531000-155531001	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs192113316	chr1:155531024-155531025	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs536430470	chr1:155531049-155531050	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs183434109	chr1:155531052-155531053	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs144157913	chr1:155531056-155531057	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs540881710	chr1:155531065-155531066	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs572425638	chr1:155531068-155531069	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs559302206	chr1:155531099-155531100	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs577298043	chr1:155531229-155531230	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs367329	chr1:155531435-155531436	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs562818169	chr1:155531475-155531476	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs558321846	chr1:155531491-155531492	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs578140007	chr1:155531523-155531524	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
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	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
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
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
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
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155507000-155530200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr1:155510600-155530200	Weak transcription	Right Ventricle	heart
3	chr1:155514400-155530200	Weak transcription	Pancreas	Pancrea
4	chr1:155514400-155530200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:155514400-155530200	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr1:155516000-155530200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr1:155517000-155531400	Weak transcription	Esophagus	oesophagus
8	chr1:155517600-155530200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:155518200-155531600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:155518600-155530000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr1:155518600-155531400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr1:155518800-155530000	Weak transcription	Stomach Smooth Muscle	stomach
13	chr1:155518800-155530200	Weak transcription	Brain Substantia Nigra	brain
14	chr1:155518800-155530200	Weak transcription	HMEC	breast
15	chr1:155519200-155530000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr1:155520200-155530200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr1:155522200-155531400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr1:155523400-155530200	Weak transcription	Fetal Kidney	kidney
19	chr1:155523600-155530000	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr1:155523800-155530200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:155524000-155530000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr1:155524000-155530200	Weak transcription	NHLF	lung
23	chr1:155524800-155530000	Weak transcription	A549	lung
24	chr1:155524800-155530200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:155525200-155530000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr1:155525600-155530000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr1:155525600-155530000	Weak transcription	Primary B cells from cord blood	blood
28	chr1:155525800-155530200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr1:155525800-155530400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr1:155526000-155530200	Weak transcription	Fetal Intestine Large	intestine
31	chr1:155526200-155531600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr1:155526200-155531800	Weak transcription	Lung	lung
33	chr1:155526600-155530200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr1:155526600-155530200	Weak transcription	Fetal Muscle Leg	muscle
35	chr1:155526600-155530400	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr1:155526600-155530600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr1:155526800-155530600	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr1:155526800-155530600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr1:155526800-155531400	Weak transcription	Fetal Muscle Trunk	muscle
40	chr1:155527600-155530000	Enhancers	Dnd41	blood
41	chr1:155527600-155530200	Enhancers	Brain Hippocampus Middle	brain
42	chr1:155527600-155530400	Enhancers	Adipose Nuclei	Adipose
43	chr1:155527600-155530600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:155527600-155530800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr1:155527800-155530800	Enhancers	Liver	Liver
46	chr1:155528000-155530200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:155528000-155530200	Weak transcription	HUVEC	blood vessel
48	chr1:155528200-155530000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr1:155528200-155530000	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr1:155528200-155530200	Enhancers	Colon Smooth Muscle	Colon

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