Variant report

Variant	nsv833396
Chromosome Location	chr17:20029183-20150808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1844)
CpG islands
(count:1830)
Chromatin interactive
region (count:111)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1844 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:20093309-20093612	K562	blood:	n/a	n/a
2	ARID3A	chr17:20129142-20129366	K562	blood:	n/a	n/a
3	ARID3A	chr17:20059136-20059256	K562	blood:	n/a	n/a
4	ARID3A	chr17:20130052-20130393	K562	blood:	n/a	n/a
5	ARID3A	chr17:20110439-20111125	K562	blood:	n/a	n/a
6	ATF2	chr17:20130036-20130451	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr17:20058419-20059429	GM12878	blood:	n/a	n/a
8	ATF2	chr17:20058615-20059310	GM12878	blood:	n/a	n/a
9	BACH1	chr17:20090476-20090702	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr17:20088179-20088586	K562	blood:	n/a	n/a
11	BACH1	chr17:20059633-20059922	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr17:20078105-20078137	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr17:20088046-20088596	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr17:20119585-20119856	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr17:20058917-20059433	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr17:20127222-20127526	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr17:20132266-20132473	GM12878	blood:	n/a	n/a
18	BATF	chr17:20137775-20138041	GM12878	blood:	n/a	n/a
19	BATF	chr17:20058437-20059307	GM12878	blood:	n/a	n/a
20	BATF	chr17:20058510-20058896	GM12878	blood:	n/a	n/a
21	BCL11A	chr17:20058856-20059315	GM12878	blood:	n/a	n/a
22	BCL11A	chr17:20058472-20058844	GM12878	blood:	n/a	n/a
23	BCL11A	chr17:20107250-20107565	GM12878	blood:	n/a	n/a
24	BCL3	chr17:20130009-20130507	A549	lung:	n/a	n/a
25	BCL3	chr17:20140915-20141180	GM12878	blood:	n/a	n/a
26	BCL3	chr17:20058724-20059784	A549	lung:	n/a	n/a
27	BCL3	chr17:20058926-20059474	GM12878	blood:	n/a	n/a
28	BCL3	chr17:20109832-20110342	A549	lung:	n/a	n/a
29	BCL3	chr17:20139141-20139466	GM12878	blood:	n/a	chr17:20139361-20139370
30	BCL3	chr17:20140911-20141229	GM12878	blood:	n/a	n/a
31	BCLAF1	chr17:20058773-20059391	GM12878	blood:	n/a	n/a
32	BHLHE40	chr17:20060075-20060316	HepG2	liver:	n/a	chr17:20060204-20060217 chr17:20060206-20060215 chr17:20060205-20060214
33	BHLHE40	chr17:20058529-20060512	GM12878	blood:	n/a	chr17:20060204-20060217 chr17:20059224-20059240 chr17:20060206-20060215 chr17:20059567-20059583 chr17:20060205-20060214
34	BHLHE40	chr17:20088371-20088669	K562	blood:	n/a	n/a
35	BHLHE40	chr17:20058838-20060389	K562	blood:	n/a	chr17:20060204-20060217 chr17:20059224-20059240 chr17:20060206-20060215 chr17:20059567-20059583 chr17:20060205-20060214
36	BHLHE40	chr17:20130089-20130330	K562	blood:	n/a	n/a
37	BHLHE40	chr17:20044564-20044677	K562	blood:	n/a	n/a
38	BRCA1	chr17:20109414-20110344	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr17:20059756-20059925	GM12878	blood:	n/a	n/a
40	BRCA1	chr17:20058470-20058485	GM12878	blood:	n/a	n/a
41	BRCA1	chr17:20059057-20059999	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr17:20059528-20059725	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr17:20099360-20100278	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr17:20077815-20078284	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr17:20098102-20098357	K562	blood:	n/a	n/a
46	CBX3	chr17:20088305-20088635	K562	blood:	n/a	n/a
47	CBX3	chr17:20058917-20059316	K562	blood:	n/a	n/a
48	CBX3	chr17:20099554-20100007	K562	blood:	n/a	n/a
49	CBX3	chr17:20108390-20108652	K562	blood:	n/a	n/a
50	CBX3	chr17:20098014-20098369	K562	blood:	n/a	n/a

(count:1830 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20059029-20059079	NH-A	brain:	n/a
2	chr17:20059957-20060007	ProgFib	skin:	n/a
3	chr17:20107320-20107370	PANC-1	pancreas:	n/a
4	chr17:20059331-20059381	ECC-1	luminal epithelium:	n/a
5	chr17:20060038-20060088	NHDF-neo	bronchial:	n/a
6	chr17:20030912-20030962	MCF-7	breast:	n/a
7	chr17:20039457-20039507	HUVEC	blood vessel:	n/a
8	chr17:20060038-20060088	SK-N-MC	brain:	n/a
9	chr17:20120115-20120165	HAEpiC	amniotic membrane:	n/a
10	chr17:20059331-20059381	IMR90	lung:	fetal
11	chr17:20060038-20060088	Jurkat	blood:	n/a
12	chr17:20060038-20060088	U87	brain:	n/a
13	chr17:20056493-20056543	HAEpiC	amniotic membrane:	n/a
14	chr17:20059411-20059461	HEEpiC	esophagus:	n/a
15	chr17:20076850-20076900	Caco-2	colon:	n/a
16	chr17:20107320-20107370	Jurkat	blood:	n/a
17	chr17:20056493-20056543	GM12891	blood:	n/a
18	chr17:20105626-20105676	HEEpiC	esophagus:	n/a
19	chr17:20107320-20107370	SAEC	small airway:	n/a
20	chr17:20044324-20044374	ProgFib	skin:	n/a
21	chr17:20059411-20059461	HRE	kidney:	n/a
22	chr17:20059137-20059187	CMK	blood:	n/a
23	chr17:20120115-20120165	HRE	kidney:	n/a
24	chr17:20059331-20059381	K562	blood:	n/a
25	chr17:20062064-20062114	HCPEpiC	choroid plexus:	n/a
26	chr17:20105626-20105676	U87	brain:	n/a
27	chr17:20056493-20056543	PFSK-1	brain:	n/a
28	chr17:20059234-20059284	IMR90	lung:	fetal
29	chr17:20120115-20120165	A549	lung:	n/a
30	chr17:20058819-20058869	AG09309	skin:	n/a
31	chr17:20075915-20075965	HCPEpiC	choroid plexus:	n/a
32	chr17:20056493-20056543	SKMC	muscle:	n/a
33	chr17:20030912-20030962	Hela-S3	cervix:	n/a
34	chr17:20059137-20059187	HCF	heart:	n/a
35	chr17:20060038-20060088	A549	lung:	n/a
36	chr17:20044324-20044374	HCT-116	colon:	n/a
37	chr17:20105626-20105676	PANC-1	pancreas:	n/a
38	chr17:20030912-20030962	AG04449	skin:	fetal
39	chr17:20059137-20059187	HMEC	breast:	n/a
40	chr17:20059106-20059156	HEEpiC	esophagus:	n/a
41	chr17:20140352-20140402	SK-N-MC	brain:	n/a
42	chr17:20060457-20060507	BJ	skin:	n/a
43	chr17:20060457-20060507	GM12891	blood:	n/a
44	chr17:20030912-20030962	HUVEC	blood vessel:	n/a
45	chr17:20059054-20059104	SAEC	small airway:	n/a
46	chr17:20059238-20059288	HRCEpiC	kidney:	n/a
47	chr17:20059238-20059288	PrEC	prostate:	n/a
48	chr17:20030912-20030962	PrEC	prostate:	n/a
49	chr17:20105626-20105676	HNPCEpiC	eye:	n/a
50	chr17:20059137-20059187	A549	lung:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:20080906..20083704-chr17:20086823..20088345,2	MCF-7	breast:
2	chr17:20044456..20046022-chr17:20048432..20050400,2	K562	blood:
3	chr17:20074412..20077021-chr17:20078655..20080833,2	K562	blood:
4	chr17:20116998..20118634-chr17:20126553..20129376,2	K562	blood:
5	chr17:20025221..20027004-chr17:20127712..20130710,2	MCF-7	breast:
6	chr17:20051458..20053031-chr17:20053497..20055897,2	MCF-7	breast:
7	chr17:20092981..20095104-chr17:20106076..20107735,2	MCF-7	breast:
8	chr17:20058383..20060895-chr17:20129200..20131943,2	K562	blood:
9	chr17:20089910..20092717-chr17:20126449..20128094,2	MCF-7	breast:
10	chr17:20099390..20102374-chr17:20106721..20109465,2	MCF-7	breast:
11	chr17:20076421..20078642-chr17:20093873..20095852,2	K562	blood:
12	chr17:20044857..20047131-chr17:20049325..20051781,3	MCF-7	breast:
13	chr17:20071385..20073993-chr17:20080012..20082353,2	MCF-7	breast:
14	chr17:20063115..20065572-chr17:20066389..20068846,2	MCF-7	breast:
15	chr17:20077595..20080145-chr17:20083243..20085538,2	MCF-7	breast:
16	chr17:20058442..20060889-chr17:20076790..20079577,2	K562	blood:
17	chr17:20090600..20093131-chr17:20093995..20097468,3	MCF-7	breast:
18	chr17:20058693..20060833-chr17:20107962..20111201,3	MCF-7	breast:
19	chr17:20058428..20060847-chr17:20086296..20087975,2	MCF-7	breast:
20	chr17:20057951..20061755-chr17:20075070..20081270,10	MCF-7	breast:
21	chr17:20057192..20060270-chr17:20108096..20110844,3	K562	blood:
22	chr17:20080496..20083311-chr17:20083511..20085814,2	MCF-7	breast:
23	chr17:20075874..20079142-chr17:20086103..20089019,5	MCF-7	breast:
24	chr17:20063491..20068167-chr17:20071822..20078082,7	MCF-7	breast:
25	chr17:20026531..20029286-chr17:20029731..20031735,2	MCF-7	breast:
26	chr17:20144551..20147091-chr17:20150035..20152753,2	MCF-7	breast:
27	chr17:20108645..20112421-chr17:20113678..20117792,3	MCF-7	breast:
28	chr17:20044620..20046385-chr17:20057505..20060250,2	MCF-7	breast:
29	chr1:151253915..151254758-chr17:20058799..20059680,2	Hela-S3	cervix:
30	chr17:20092728..20094832-chr17:20098161..20099795,2	K562	blood:
31	chr17:20056629..20058673-chr17:20092649..20094964,2	MCF-7	breast:
32	chr17:20059180..20059804-chr5:108745357..108746183,2	Hela-S3	cervix:
33	chr17:20144551..20147091-chr17:20150035..20152753,2	MCF-7	breast:
34	chr17:20080334..20082016-chr17:20102428..20104693,2	MCF-7	breast:
35	chr17:20076969..20079576-chr17:20080631..20082312,2	MCF-7	breast:
36	chr17:20109966..20112285-chr17:20118187..20119843,2	MCF-7	breast:
37	chr17:20109966..20112285-chr17:20118187..20119843,2	MCF-7	breast:
38	chr17:20074035..20075554-chr17:20084384..20086297,2	MCF-7	breast:
39	chr17:20044857..20047131-chr17:20049325..20051781,3	MCF-7	breast:
40	chr17:20058977..20061113-chr17:20127273..20129010,3	MCF-7	breast:
41	chr17:20088001..20089506-chr17:20108427..20110013,2	MCF-7	breast:
42	chr17:20069675..20071454-chr17:20074392..20077634,3	MCF-7	breast:
43	chr17:20051699..20054406-chr17:20055963..20057917,2	K562	blood:
44	chr17:19878871..19883594-chr17:20057277..20060362,4	K562	blood:
45	chr17:20057192..20060270-chr17:20108096..20110844,3	K562	blood:
46	chr17:20097809..20099634-chr17:20110030..20112138,2	K562	blood:
47	chr17:20097809..20099634-chr17:20110030..20112138,2	K562	blood:
48	chr17:20076826..20080402-chr17:20081688..20085232,6	K562	blood:
49	chr17:20041429..20043653-chr17:20055230..20057958,2	K562	blood:
50	chr17:20092728..20094832-chr17:20098161..20099795,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPECC1-1	chr17:20088395-20088499	ENSG00000263494.1

No data

Variant related genes	Relation type
ENSG00000263494	TF binding region
RNU6-258P	TF binding region
SPECC1	TF binding region
ENSG00000263494	CpG island
RNU6-258P	CpG island
SPECC1	CpG island
ENSG00000212186	chromatin interactions
ENSG00000128487	chromatin interactions
ENSG00000108599	chromatin interactions
ENSG00000154898	chromatin interactions
ENSG00000263494	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000198961	chromatin interactions
ENSG00000232671	chromatin interactions

Extended variants
information (count: 4477 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:4477 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147164060	chr17:20029186-20029187	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs148363150	chr17:20029208-20029209	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs16960700	chr17:20029225-20029226	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs549842899	chr17:20029300-20029301	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80123538	chr17:20029315-20029316	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35519944	chr17:20029324-20029325	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183753354	chr17:20029340-20029341	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558413078	chr17:20029347-20029348	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs571811972	chr17:20029353-20029354	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534425524	chr17:20029387-20029388	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369516677	chr17:20029400-20029401	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558147415	chr17:20029431-20029432	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573803750	chr17:20029525-20029526	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542711158	chr17:20029527-20029528	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs199539676	chr17:20029537-20029538	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556168693	chr17:20029538-20029539	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576371869	chr17:20029548-20029549	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545041486	chr17:20029567-20029568	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565206576	chr17:20029573-20029574	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111482596	chr17:20029585-20029586	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs11868116	chr17:20029593-20029594	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs537149134	chr17:20029610-20029611	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150914439	chr17:20029661-20029662	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529861369	chr17:20029705-20029706	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370588053	chr17:20029708-20029709	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549880019	chr17:20029769-20029770	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569584884	chr17:20029778-20029779	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372306343	chr17:20029826-20029827	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs532146782	chr17:20029830-20029831	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs551856473	chr17:20029852-20029853	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs573785292	chr17:20029853-20029854	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374676201	chr17:20029865-20029866	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs537646792	chr17:20029869-20029870	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs4588033	chr17:20029901-20029902	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs534180723	chr17:20029921-20029922	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs8077051	chr17:20029933-20029934	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs567500315	chr17:20029953-20029954	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115235492	chr17:20029955-20029956	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556635970	chr17:20029977-20029978	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576431565	chr17:20030016-20030017	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545388719	chr17:20030102-20030103	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558640116	chr17:20030119-20030120	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572346911	chr17:20030181-20030182	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114369275	chr17:20030271-20030272	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs561092855	chr17:20030331-20030332	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs529898508	chr17:20030344-20030345	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs543607405	chr17:20030395-20030396	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563416703	chr17:20030424-20030425	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139391686	chr17:20030450-20030451	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74654653	chr17:20030461-20030462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:154)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Medulloblastoma	16783165	CNVD

Chromatin state (count:3185 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19999000-20032800	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr17:20002200-20033400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr17:20025400-20040400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr17:20025600-20031000	Weak transcription	Left Ventricle	heart
5	chr17:20025600-20034600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr17:20025800-20029200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr17:20025800-20029800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr17:20025800-20030200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr17:20025800-20031000	Weak transcription	Hela-S3	cervix
10	chr17:20025800-20037600	Weak transcription	Ovary	ovary
11	chr17:20025800-20044400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr17:20026000-20031000	Weak transcription	Fetal Brain Female	brain
13	chr17:20026000-20031400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr17:20026200-20040000	Weak transcription	Aorta	Aorta
15	chr17:20026200-20049800	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr17:20026600-20031200	Weak transcription	Fetal Brain Male	brain
17	chr17:20026600-20033200	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr17:20027000-20031000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr17:20028600-20029400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr17:20028600-20029600	Genic enhancers	Brain Cingulate Gyrus	brain
21	chr17:20028600-20029800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr17:20028600-20030200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr17:20028800-20029400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr17:20028800-20029400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr17:20028800-20029400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr17:20028800-20029400	Enhancers	NHLF	lung
27	chr17:20028800-20029600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr17:20028800-20029600	Enhancers	Adipose Nuclei	Adipose
29	chr17:20028800-20030000	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr17:20028800-20030000	Enhancers	Brain Substantia Nigra	brain
31	chr17:20028800-20030200	Enhancers	Brain Anterior Caudate	brain
32	chr17:20028800-20031600	Enhancers	Brain Angular Gyrus	brain
33	chr17:20029000-20029200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr17:20029000-20029600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr17:20029000-20030000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr17:20029000-20030200	Enhancers	Brain Hippocampus Middle	brain
37	chr17:20029200-20029400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr17:20029400-20029800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr17:20029400-20030200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr17:20029400-20030800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr17:20029400-20030800	Weak transcription	NHLF	lung
42	chr17:20029400-20033200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr17:20029400-20033600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr17:20029400-20042400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr17:20029600-20030000	Weak transcription	Adipose Nuclei	Adipose
46	chr17:20029600-20031000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr17:20029600-20031200	Weak transcription	Brain Cingulate Gyrus	brain
48	chr17:20029600-20058800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr17:20029800-20031800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr17:20029800-20032000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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