Variant report

Variant	nsv946421
Chromosome Location	chr1:155656230-155659076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:617)
CpG islands
(count:671)
Chromatin interactive
region (count:27)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:155658644-155658844	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:155658506-155658881	K562	blood:	n/a	n/a
3	ATF2	chr1:155658524-155659058	GM12878	blood:	n/a	n/a
4	ATF2	chr1:155657966-155658413	GM12878	blood:	n/a	n/a
5	ATF3	chr1:155658307-155659029	A549	lung:	n/a	n/a
6	BACH1	chr1:155658661-155658693	K562	blood:	n/a	n/a
7	BACH1	chr1:155657984-155659056	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr1:155657407-155657795	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:155657352-155657700	GM12878	blood:	n/a	n/a
10	BCL3	chr1:155657883-155658436	A549	lung:	n/a	n/a
11	BCL3	chr1:155658481-155658924	A549	lung:	n/a	n/a
12	BCLAF1	chr1:155657814-155658689	GM12878	blood:	n/a	n/a
13	BCLAF1	chr1:155657912-155658523	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:155658487-155658957	A549	lung:	n/a	n/a
15	BHLHE40	chr1:155658190-155659012	HepG2	liver:	n/a	n/a
16	BHLHE40	chr1:155658013-155658987	GM12878	blood:	n/a	n/a
17	BHLHE40	chr1:155658035-155659053	K562	blood:	n/a	n/a
18	BRCA1	chr1:155658595-155658851	HepG2	liver:	n/a	n/a
19	BRCA1	chr1:155658263-155658949	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr1:155658456-155658910	GM12878	blood:	n/a	n/a
21	CBX3	chr1:155657884-155659471	K562	blood:	n/a	n/a
22	CCNT2	chr1:155658024-155658906	K562	blood:	n/a	n/a
23	CEBPB	chr1:155658676-155658996	GM12878	blood:	n/a	n/a
24	CEBPB	chr1:155658093-155658136	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:155658528-155659266	GM12878	blood:	n/a	n/a
26	CEBPB	chr1:155658443-155658948	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr1:155658218-155659207	K562	blood:	n/a	n/a
28	CEBPD	chr1:155658309-155658650	HepG2	liver:	n/a	n/a
29	CHD1	chr1:155657886-155659040	GM12878	blood:	n/a	chr1:155658567-155658577
30	CHD1	chr1:155657643-155659334	IMR90	lung:	n/a	chr1:155658567-155658577
31	CHD1	chr1:155658348-155658952	H1-hESC	embryonic stem cell:	n/a	chr1:155658567-155658577
32	CHD2	chr1:155658077-155658953	Hela-S3	cervix:	n/a	chr1:155658567-155658577
33	CHD2	chr1:155658475-155658911	HepG2	liver:	n/a	chr1:155658567-155658577
34	CHD2	chr1:155658017-155658965	GM12878	blood:	n/a	chr1:155658567-155658577
35	CHD2	chr1:155657937-155658127	HepG2	liver:	n/a	n/a
36	CHD2	chr1:155658040-155658812	K562	blood:	n/a	chr1:155658567-155658577
37	CREB1	chr1:155657958-155659096	HepG2	liver:	n/a	n/a
38	CREB1	chr1:155657956-155659005	GM12878	blood:	n/a	n/a
39	CREB1	chr1:155657960-155659027	A549	lung:	n/a	n/a
40	CTBP2	chr1:155658200-155659009	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr1:155658480-155658630	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr1:155658640-155658790	HEK293	kidney:	n/a	n/a
43	CTCF	chr1:155658480-155658630	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr1:155658620-155658770	GM12865	blood:	n/a	n/a
45	CTCF	chr1:155657780-155657930	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr1:155658180-155658330	GM12869	blood:	n/a	n/a
47	CTCF	chr1:155658760-155658910	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr1:155658600-155658750	Caco-2	colon:	n/a	n/a
49	CTCF	chr1:155657900-155658050	BJ	skin:	n/a	n/a
50	CTCF	chr1:155658120-155658270	SK-N-SH_RA	brain:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:155658929-155658979	T-47D	breast:	n/a
2	chr1:155658701-155658751	SKMC	muscle:	n/a
3	chr1:155657930-155657980	HCF	heart:	n/a
4	chr1:155658898-155658948	Jurkat	blood:	n/a
5	chr1:155658835-155658885	Hela-S3	cervix:	n/a
6	chr1:155658214-155658264	HCM	heart:	n/a
7	chr1:155658933-155658983	Caco-2	colon:	n/a
8	chr1:155658214-155658264	ProgFib	skin:	n/a
9	chr1:155658214-155658264	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:155658576-155658626	GM12878	blood:	n/a
11	chr1:155658701-155658751	ovcar-3	ovarian:	n/a
12	chr1:155658843-155658893	HRCEpiC	kidney:	n/a
13	chr1:155658835-155658885	BE2_C	brain:	n/a
14	chr1:155658898-155658948	HEEpiC	esophagus:	n/a
15	chr1:155658843-155658893	T-47D	breast:	n/a
16	chr1:155658214-155658264	Caco-2	colon:	n/a
17	chr1:155658576-155658626	HEEpiC	esophagus:	n/a
18	chr1:155658509-155658559	RPTEC	kidney:	n/a
19	chr1:155658835-155658885	NT2-D1	testis:	n/a
20	chr1:155658933-155658983	U87	brain:	n/a
21	chr1:155658142-155658192	HRE	kidney:	n/a
22	chr1:155658509-155658559	HL-60	blood:	n/a
23	chr1:155658898-155658948	HUVEC	blood vessel:	n/a
24	chr1:155658929-155658979	A549	lung:	n/a
25	chr1:155658898-155658948	SK-N-SH	brain:	n/a
26	chr1:155658214-155658264	NHDF-neo	bronchial:	n/a
27	chr1:155658933-155658983	Hepatocyte	liver:	n/a
28	chr1:155658509-155658559	BJ	skin:	n/a
29	chr1:155658843-155658893	Hela-S3	cervix:	n/a
30	chr1:155658933-155658983	HRE	kidney:	n/a
31	chr1:155658142-155658192	HIPEpiC	eye:	n/a
32	chr1:155657930-155657980	T-47D	breast:	n/a
33	chr1:155657930-155657980	U87	brain:	n/a
34	chr1:155658835-155658885	A549	lung:	n/a
35	chr1:155658509-155658559	GM12892	blood:	n/a
36	chr1:155657930-155657980	NB4	blood:	n/a
37	chr1:155657930-155657980	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:155658898-155658948	HNPCEpiC	eye:	n/a
39	chr1:155658843-155658893	ECC-1	luminal epithelium:	n/a
40	chr1:155658701-155658751	HRCEpiC	kidney:	n/a
41	chr1:155658929-155658979	NH-A	brain:	n/a
42	chr1:155658142-155658192	PrEC	prostate:	n/a
43	chr1:155658701-155658751	HIPEpiC	eye:	n/a
44	chr1:155658509-155658559	HUVEC	blood vessel:	n/a
45	chr1:155658214-155658264	CMK	blood:	n/a
46	chr1:155658509-155658559	HRPEpiC	eye:	n/a
47	chr1:155658142-155658192	SAEC	small airway:	n/a
48	chr1:155658142-155658192	HCF	heart:	n/a
49	chr1:155658843-155658893	A549	lung:	n/a
50	chr1:155658701-155658751	HNPCEpiC	eye:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155647841..155650282-chr1:155658064..155659902,2	MCF-7	breast:
2	chr1:155646937..155653370-chr1:155653884..155660272,11	K562	blood:
3	chr1:155532088..155532960-chr1:155658209..155658720,2	MCF-7	breast:
4	chr1:155532081..155532969-chr1:155658202..155658825,5	HCT-116	colon:
5	chr1:155293644..155295180-chr1:155658200..155659752,2	MCF-7	breast:
6	chr1:155657873..155658675-chr15:91415725..91416297,2	Hela-S3	cervix:
7	chr1:155658041..155658876-chr9:75766420..75767093,2	Hela-S3	cervix:
8	chr1:155532102..155532798-chr1:155657720..155658726,4	NB4	blood:
9	chr1:155658615..155659548-chr3:138312824..138313654,2	Hela-S3	cervix:
10	chr1:155195691..155197531-chr1:155658226..155660788,2	K562	blood:
11	chr1:155658633..155662039-chr1:156022948..156025065,3	K562	blood:
12	chr1:155530812..155532531-chr1:155657028..155659724,4	K562	blood:
13	chr1:155619948..155622617-chr1:155654194..155656266,2	MCF-7	breast:
14	chr1:155657577..155658554-chr17:56736530..56737192,2	MCF-7	breast:
15	chr1:155652988..155656346-chr1:155657323..155660504,4	MCF-7	breast:
16	chr1:155649685..155651482-chr1:155656249..155657899,2	MCF-7	breast:
17	chr1:155644991..155647996-chr1:155653884..155656777,3	MCF-7	breast:
18	chr1:155658521..155660214-chr1:164740544..164742861,2	MCF-7	breast:
19	chr1:155531168..155533264-chr1:155658199..155660031,3	MCF-7	breast:
20	chr1:155656761..155658571-chr1:155822378..155824933,2	K562	blood:
21	chr1:155658041..155658957-chr2:61243850..61244532,2	Hela-S3	cervix:
22	chr1:155657851..155658412-chr9:98637639..98638211,2	Hela-S3	cervix:
23	chr1:155649129..155651594-chr1:155654278..155656624,2	MCF-7	breast:
24	chr1:155658491..155659047-chr12:49658493..49659361,2	Hela-S3	cervix:
25	chr1:155621509..155623036-chr1:155655478..155657409,2	K562	blood:
26	chr1:155650232..155654143-chr1:155656732..155660370,8	MCF-7	breast:
27	chr1:155531220..155534536-chr1:155656727..155659727,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DAP3-1	chr1:155658886-155659418	NONHSAT006758
2	lnc-DAP3-1	chr1:155657751-155657983	NONHSAT006756
3	lnc-DAP3-1	chr1:155657782-155657983	NONHSAT006758
4	lnc-DAP3-1	chr1:155658630-155659128	NONHSAT006756

No data

Variant related genes	Relation type
DAP3	TF binding region
YY1AP1	TF binding region
DAP3	CpG island
YY1AP1	CpG island
ENSG00000162927	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000162928	chromatin interactions
ENSG00000185630	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000140564	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000175611	chromatin interactions
ENSG00000116539	chromatin interactions
ENSG00000182150	chromatin interactions
ENSG00000135046	chromatin interactions
ENSG00000163374	chromatin interactions
ENSG00000116586	chromatin interactions
ENSG00000116580	chromatin interactions
ENSG00000160803	chromatin interactions
ENSG00000235919	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000132676	chromatin interactions
ENSG00000114107	chromatin interactions

Extended variants
information (count: 147 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:147 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573341670	chr1:155656262-155656263	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs540750899	chr1:155656263-155656264	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs112090935	chr1:155656269-155656270	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs553181400	chr1:155656290-155656291	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs185522410	chr1:155656292-155656293	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs577801970	chr1:155656327-155656328	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs550293647	chr1:155656344-155656345	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs34215620	chr1:155656359-155656360	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs397862941	chr1:155656360-155656361	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs649147	chr1:155656398-155656399	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs563645013	chr1:155656402-155656403	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs530714993	chr1:155656434-155656435	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs561056076	chr1:155656477-155656478	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs560565722	chr1:155656484-155656485	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs397834817	chr1:155656497-155656498	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528154256	chr1:155656518-155656519	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs649971	chr1:155656556-155656557	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs141316364	chr1:155656561-155656562	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571742348	chr1:155656574-155656575	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs532787140	chr1:155656604-155656605	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550897835	chr1:155656639-155656640	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374204161	chr1:155656682-155656683	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs529707576	chr1:155656693-155656694	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs569495474	chr1:155656719-155656720	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs71628681	chr1:155656793-155656794	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs554973020	chr1:155656807-155656808	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs566899679	chr1:155656884-155656885	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs187862237	chr1:155656898-155656899	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs75256783	chr1:155656942-155656943	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs577756400	chr1:155657230-155657231	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs374895029	chr1:155657353-155657354	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs556884268	chr1:155657395-155657396	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs575459217	chr1:155657400-155657401	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs368956508	chr1:155657409-155657410	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs552081697	chr1:155657429-155657430	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs528118523	chr1:155657473-155657474	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs539940296	chr1:155657505-155657506	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs564947346	chr1:155657528-155657529	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs532117259	chr1:155657549-155657550	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs551120248	chr1:155657558-155657559	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs569374602	chr1:155657561-155657562	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs530394176	chr1:155657569-155657570	Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs548933386	chr1:155657578-155657579	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs61817760	chr1:155657628-155657629	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs566862792	chr1:155657630-155657631	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs534228686	chr1:155657645-155657646	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs552291822	chr1:155657660-155657661	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs569040520	chr1:155657688-155657689	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs537968805	chr1:155657690-155657691	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs557088744	chr1:155657700-155657701	Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
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:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155627000-155657600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:155634600-155657800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr1:155645200-155657200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr1:155646600-155657600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:155648600-155656400	Weak transcription	Fetal Kidney	kidney
6	chr1:155648600-155657200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr1:155650000-155657400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:155650000-155657600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr1:155650200-155656400	Weak transcription	HSMM	muscle
10	chr1:155650200-155656800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:155650200-155657400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr1:155650400-155657200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:155650800-155656400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:155650800-155656400	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr1:155650800-155657400	Weak transcription	Placenta	Placenta
16	chr1:155653000-155656600	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr1:155653000-155656600	Enhancers	Brain Angular Gyrus	brain
18	chr1:155653200-155656600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr1:155653200-155656800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr1:155653800-155656600	Enhancers	Primary T cells fromperipheralblood	blood
21	chr1:155653800-155657400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr1:155654000-155657400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr1:155654000-155657400	Weak transcription	Esophagus	oesophagus
24	chr1:155654000-155657600	Weak transcription	Small Intestine	intestine
25	chr1:155654600-155656600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr1:155654600-155656600	Enhancers	Liver	Liver
27	chr1:155654600-155657600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:155654800-155656400	Enhancers	Primary T cells from cord blood	blood
29	chr1:155655000-155656400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:155655000-155656400	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr1:155655000-155656400	Enhancers	Rectal Smooth Muscle	rectum
32	chr1:155655000-155656600	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr1:155655000-155656800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr1:155655000-155657000	Enhancers	Brain Substantia Nigra	brain
35	chr1:155655200-155656600	Enhancers	Brain Cingulate Gyrus	brain
36	chr1:155655200-155656600	Enhancers	Fetal Stomach	stomach
37	chr1:155655400-155659600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr1:155655600-155656400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr1:155655600-155656400	Enhancers	Primary T killer memory cells from peripheral blood	blood
40	chr1:155655600-155656400	Active TSS	Colonic Mucosa	Colon
41	chr1:155655600-155656400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr1:155655600-155656600	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr1:155655600-155657200	Enhancers	Primary B cells from cord blood	blood
44	chr1:155655800-155656400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr1:155655800-155656600	Enhancers	Primary B cells from peripheral blood	blood
46	chr1:155656000-155656400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:155656000-155656400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr1:155656000-155656400	Enhancers	Gastric	stomach
49	chr1:155656000-155656600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr1:155656000-155656600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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