Variant report

Variant	nsv482830
Chromosome Location	chr17:20012748-20169153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2480)
CpG islands
(count:2200)
Chromatin interactive
region (count:129)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

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	chr17:20130052-20130393	K562	blood:	n/a	n/a
3	ARID3A	chr17:20110439-20111125	K562	blood:	n/a	n/a
4	ARID3A	chr17:20129142-20129366	K562	blood:	n/a	n/a
5	ARID3A	chr17:20059136-20059256	K562	blood:	n/a	n/a
6	ATF1	chr17:20166977-20167251	K562	blood:	n/a	n/a
7	ATF2	chr17:20058419-20059429	GM12878	blood:	n/a	n/a
8	ATF2	chr17:20130036-20130451	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr17:20058615-20059310	GM12878	blood:	n/a	n/a
10	BACH1	chr17:20058917-20059433	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr17:20127222-20127526	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	chr17:20119585-20119856	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr17:20020015-20020505	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr17:20090476-20090702	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr17:20088046-20088596	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr17:20059633-20059922	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr17:20088179-20088586	K562	blood:	n/a	n/a
19	BACH1	chr17:20164107-20164272	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr17:20058437-20059307	GM12878	blood:	n/a	n/a
21	BATF	chr17:20058510-20058896	GM12878	blood:	n/a	n/a
22	BATF	chr17:20137775-20138041	GM12878	blood:	n/a	n/a
23	BATF	chr17:20132266-20132473	GM12878	blood:	n/a	n/a
24	BCL11A	chr17:20058856-20059315	GM12878	blood:	n/a	n/a
25	BCL11A	chr17:20107250-20107565	GM12878	blood:	n/a	n/a
26	BCL11A	chr17:20058472-20058844	GM12878	blood:	n/a	n/a
27	BCL3	chr17:20058724-20059784	A549	lung:	n/a	n/a
28	BCL3	chr17:20139141-20139466	GM12878	blood:	n/a	chr17:20139361-20139370
29	BCL3	chr17:20140911-20141229	GM12878	blood:	n/a	n/a
30	BCL3	chr17:20109832-20110342	A549	lung:	n/a	n/a
31	BCL3	chr17:20058926-20059474	GM12878	blood:	n/a	n/a
32	BCL3	chr17:20130009-20130507	A549	lung:	n/a	n/a
33	BCL3	chr17:20140915-20141180	GM12878	blood:	n/a	n/a
34	BCL3	chr17:20026914-20027278	GM12878	blood:	n/a	n/a
35	BCLAF1	chr17:20019949-20020351	GM12878	blood:	n/a	n/a
36	BCLAF1	chr17:20058773-20059391	GM12878	blood:	n/a	n/a
37	BHLHE40	chr17:20044564-20044677	K562	blood:	n/a	n/a
38	BHLHE40	chr17:20166944-20167199	K562	blood:	n/a	n/a
39	BHLHE40	chr17:20058529-20060512	GM12878	blood:	n/a	chr17:20060204-20060217 chr17:20059224-20059240 chr17:20060206-20060215 chr17:20059567-20059583 chr17:20060205-20060214
40	BHLHE40	chr17:20130089-20130330	K562	blood:	n/a	n/a
41	BHLHE40	chr17:20060075-20060316	HepG2	liver:	n/a	chr17:20060204-20060217 chr17:20060206-20060215 chr17:20060205-20060214
42	BHLHE40	chr17:20088371-20088669	K562	blood:	n/a	n/a
43	BHLHE40	chr17:20024974-20025288	GM12878	blood:	n/a	n/a
44	BHLHE40	chr17:20058838-20060389	K562	blood:	n/a	chr17:20060204-20060217 chr17:20059224-20059240 chr17:20060206-20060215 chr17:20059567-20059583 chr17:20060205-20060214
45	BRCA1	chr17:20099360-20100278	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr17:20109414-20110344	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr17:20059528-20059725	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr17:20059756-20059925	GM12878	blood:	n/a	n/a
49	BRCA1	chr17:20077815-20078284	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr17:20059057-20059999	Hela-S3	cervix:	n/a	n/a

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20059327-20059377	T-47D	breast:	n/a
2	chr17:20120115-20120165	LNCaP	prostate:	n/a
3	chr17:20075915-20075965	BJ	skin:	n/a
4	chr17:20044324-20044374	SK-N-SH_RA	brain:	n/a
5	chr17:20059327-20059377	T-47D	breast:	n/a
6	chr17:20120115-20120165	LNCaP	prostate:	n/a
7	chr17:20075915-20075965	BJ	skin:	n/a
8	chr17:20044324-20044374	SK-N-SH_RA	brain:	n/a
9	chr17:20059054-20059104	H1-hESC	embryonic stem cell:	embryo
10	chr17:20058819-20058869	NB4	blood:	n/a
11	chr17:20060457-20060507	SK-N-MC	brain:	n/a
12	chr17:20059234-20059284	AG09319	gingival:	n/a
13	chr17:20059327-20059377	ProgFib	skin:	n/a
14	chr17:20059957-20060007	BJ	skin:	n/a
15	chr17:20013829-20013879	Hepatocyte	liver:	n/a
16	chr17:20059234-20059284	HAEpiC	amniotic membrane:	n/a
17	chr17:20059957-20060007	AG09319	gingival:	n/a
18	chr17:20140352-20140402	SK-N-MC	brain:	n/a
19	chr17:20128997-20129047	HCM	heart:	n/a
20	chr17:20140352-20140402	HEK293	kidney:	embryo
21	chr17:20059225-20059275	HCM	heart:	n/a
22	chr17:20039457-20039507	AG10803	skin:	n/a
23	chr17:20059234-20059284	HIPEpiC	eye:	n/a
24	chr17:20060311-20060361	NHDF-neo	bronchial:	n/a
25	chr17:20030912-20030962	HepG2	liver:	n/a
26	chr17:20105626-20105676	MCF-7	breast:	n/a
27	chr17:20059225-20059275	AoSMC	blood vessel:	n/a
28	chr17:20059227-20059277	CMK	blood:	n/a
29	chr17:20059234-20059284	HMEC	breast:	n/a
30	chr17:20059327-20059377	HEEpiC	esophagus:	n/a
31	chr17:20059054-20059104	CMK	blood:	n/a
32	chr17:20059029-20059079	CMK	blood:	n/a
33	chr17:20059331-20059381	AG09309	skin:	n/a
34	chr17:20059227-20059277	MCF10A-Er-Src	breast:	n/a
35	chr17:20105626-20105676	PFSK-1	brain:	n/a
36	chr17:20105626-20105676	A549	lung:	n/a
37	chr17:20059234-20059284	T-47D	breast:	n/a
38	chr17:20156940-20156990	HEK293	kidney:	embryo
39	chr17:20107320-20107370	GM06990	blood:	n/a
40	chr17:20030912-20030962	T-47D	breast:	n/a
41	chr17:20013887-20013937	GM12891	blood:	n/a
42	chr17:20059411-20059461	PANC-1	pancreas:	n/a
43	chr17:20060457-20060507	AG09309	skin:	n/a
44	chr17:20059227-20059277	NH-A	brain:	n/a
45	chr17:20060457-20060507	GM12878	blood:	n/a
46	chr17:20059225-20059275	HCPEpiC	choroid plexus:	n/a
47	chr17:20013887-20013937	AG10803	skin:	n/a
48	chr17:20060457-20060507	U87	brain:	n/a
49	chr17:20059238-20059288	HEK293	kidney:	embryo
50	chr17:20059331-20059381	HCT-116	colon:	n/a

(count:129 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:20076826..20080402-chr17:20081688..20085232,6	K562	blood:
2	chr17:20108645..20112421-chr17:20113678..20117792,3	MCF-7	breast:
3	chr17:20063488..20065796-chr17:20068015..20069552,2	K562	blood:
4	chr17:20099390..20102374-chr17:20106721..20109465,2	MCF-7	breast:
5	chr17:20088001..20089506-chr17:20108427..20110013,2	MCF-7	breast:
6	chr17:20057984..20061939-chr17:20062110..20066958,6	K562	blood:
7	chr17:20063488..20065796-chr17:20068015..20069552,2	K562	blood:
8	chr17:20075874..20079142-chr17:20086103..20089019,5	MCF-7	breast:
9	chr17:20058693..20060833-chr17:20107962..20111201,3	MCF-7	breast:
10	chr17:20025221..20027004-chr17:20127712..20130710,2	MCF-7	breast:
11	chr17:20109966..20112285-chr17:20118187..20119843,2	MCF-7	breast:
12	chr17:19688891..19689853-chr17:20019794..20020671,3	MCF-7	breast:
13	chr17:20071385..20073993-chr17:20080012..20082353,2	MCF-7	breast:
14	chr17:20092981..20095104-chr17:20106076..20107735,2	MCF-7	breast:
15	chr17:20086231..20089170-chr17:20090433..20092897,2	MCF-7	breast:
16	chr17:20080496..20083311-chr17:20083511..20085814,2	MCF-7	breast:
17	chr17:20080906..20083704-chr17:20086823..20088345,2	MCF-7	breast:
18	chr17:20044857..20047131-chr17:20049325..20051781,3	MCF-7	breast:
19	chr17:20061838..20064819-chr17:20072515..20074758,3	MCF-7	breast:
20	chr17:20051699..20054406-chr17:20055963..20057917,2	K562	blood:
21	chr17:20027673..20031271-chr17:20059449..20061879,3	MCF-7	breast:
22	chr17:19881156..19883404-chr17:20076663..20078909,2	MCF-7	breast:
23	chr17:20074412..20077021-chr17:20078655..20080833,2	K562	blood:
24	chr17:20109966..20112285-chr17:20118187..20119843,2	MCF-7	breast:
25	chr17:20020458..20023220-chr17:20026359..20029161,2	K562	blood:
26	chr17:20089910..20092717-chr17:20126449..20128094,2	MCF-7	breast:
27	chr17:20144551..20147091-chr17:20150035..20152753,2	MCF-7	breast:
28	chr17:19895701..19896691-chr17:20019722..20020794,7	K562	blood:
29	chr17:20056629..20058673-chr17:20092649..20094964,2	MCF-7	breast:
30	chr17:20164807..20165435-chr17:20223847..20224473,2	MCF-7	breast:
31	chr17:20071385..20073993-chr17:20080012..20082353,2	MCF-7	breast:
32	chr17:20076826..20080402-chr17:20081688..20085232,6	K562	blood:
33	chr17:20108704..20111495-chr17:20125977..20128241,2	MCF-7	breast:
34	chr17:20044620..20046385-chr17:20057505..20060250,2	MCF-7	breast:
35	chr17:20063491..20068167-chr17:20071822..20078082,7	MCF-7	breast:
36	chr17:20058426..20061680-chr17:20114068..20117694,3	MCF-7	breast:
37	chr17:20063115..20065572-chr17:20066389..20068846,2	MCF-7	breast:
38	chr17:20097809..20099634-chr17:20110030..20112138,2	K562	blood:
39	chr17:20144165..20146631-chr17:20158234..20160364,2	MCF-7	breast:
40	chr17:20051458..20053031-chr17:20053497..20055897,2	MCF-7	breast:
41	chr17:20109094..20109672-chr17:20129868..20130670,2	K562	blood:
42	chr17:20026531..20029286-chr17:20029731..20031735,2	MCF-7	breast:
43	chr17:20074035..20075554-chr17:20084384..20086297,2	MCF-7	breast:
44	chr17:20025519..20027305-chr17:20058303..20059894,2	MCF-7	breast:
45	chr17:20036574..20039252-chr17:20057707..20061557,6	MCF-7	breast:
46	chr17:20057342..20059768-chr17:20130709..20132708,3	MCF-7	breast:
47	chr17:20089910..20092717-chr17:20126449..20128094,2	MCF-7	breast:
48	chr17:20057192..20060270-chr17:20108096..20110844,3	K562	blood:
49	chr17:20059521..20061143-chr17:20081573..20083266,2	MCF-7	breast:
50	chr17:20080334..20082016-chr17:20102428..20104693,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPECC1-1	chr17:20088395-20088499	ENSG00000263494.1
2	lnc-CCDC144C-3	chr17:20015137-20016303	NONHSAT146542

No data

Variant related genes	Relation type
KCTD9P1	TF binding region
ENSG00000263494	TF binding region
RNU6-258P	TF binding region
SPECC1	TF binding region
KCTD9P1	CpG island
ENSG00000263494	CpG island
RNU6-258P	CpG island
SPECC1	CpG island
ENSG00000212186	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000128487	chromatin interactions
ENSG00000261033	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000263494	chromatin interactions
ENSG00000108599	chromatin interactions
ENSG00000198961	chromatin interactions
ENSG00000154898	chromatin interactions

Extended variants
information (count: 5772 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:5772 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548627116	chr17:20012836-20012837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs568754725	chr17:20012862-20012863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185489776	chr17:20012880-20012881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531075364	chr17:20012963-20012964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147036362	chr17:20012989-20012990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189659473	chr17:20013025-20013026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553493644	chr17:20013089-20013090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566907799	chr17:20013090-20013091	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183919809	chr17:20013097-20013098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555447771	chr17:20013110-20013111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7213349	chr17:20013139-20013140	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs542912933	chr17:20013141-20013142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544140455	chr17:20013194-20013195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372315845	chr17:20013211-20013212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs199855578	chr17:20013260-20013261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147656391	chr17:20013271-20013272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539971922	chr17:20013273-20013274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142336281	chr17:20013305-20013306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554393767	chr17:20013368-20013369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528951727	chr17:20013381-20013382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527253332	chr17:20013390-20013391	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs58241313	chr17:20013410-20013411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542621470	chr17:20013429-20013430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4925086	chr17:20013459-20013460	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs111840738	chr17:20013460-20013461	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs531239902	chr17:20013465-20013466	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs551291802	chr17:20013466-20013467	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs544686844	chr17:20013500-20013501	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs543343006	chr17:20013531-20013532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188914457	chr17:20013557-20013558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs533552346	chr17:20013623-20013624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs35887699	chr17:20013654-20013655	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34068493	chr17:20013661-20013662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547146311	chr17:20013673-20013674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553802962	chr17:20013684-20013685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566993284	chr17:20013688-20013689	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374663900	chr17:20013745-20013746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150748271	chr17:20013747-20013748	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368953489	chr17:20013791-20013792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371467650	chr17:20013795-20013796	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs3764436	chr17:20013802-20013803	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs141316021	chr17:20013818-20013819	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs199761506	chr17:20013828-20013829	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549370405	chr17:20013829-20013830	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs201890028	chr17:20013850-20013851	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs142403984	chr17:20013857-20013858	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs200914041	chr17:20013858-20013859	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs145933122	chr17:20013859-20013860	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs538188184	chr17:20013863-20013864	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs372374636	chr17:20013882-20013883	Bivalent/Poised TSS Strong transcription Weak 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:4063 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:19999000-20032800	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr17:20002200-20018800	Weak transcription	Spleen	Spleen
3	chr17:20002200-20033400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr17:20002400-20013600	Weak transcription	Aorta	Aorta
5	chr17:20004000-20013600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr17:20007000-20013400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr17:20007000-20013600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr17:20007200-20013600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr17:20007400-20013600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr17:20007400-20013600	Weak transcription	Ovary	ovary
11	chr17:20007400-20015000	Weak transcription	Adipose Nuclei	Adipose
12	chr17:20007400-20024200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr17:20007600-20013400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr17:20007600-20013600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr17:20007600-20019800	Weak transcription	Brain Cingulate Gyrus	brain
16	chr17:20007600-20020200	Weak transcription	Brain Angular Gyrus	brain
17	chr17:20007600-20024000	Weak transcription	Brain Substantia Nigra	brain
18	chr17:20007800-20017800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr17:20007800-20020200	Weak transcription	Brain Anterior Caudate	brain
20	chr17:20007800-20024000	Weak transcription	Brain Hippocampus Middle	brain
21	chr17:20009200-20024200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr17:20010800-20017200	Weak transcription	Primary T cells from cord blood	blood
23	chr17:20011800-20019200	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr17:20012000-20018400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr17:20012600-20013800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr17:20012600-20019800	Weak transcription	A549	lung
27	chr17:20013400-20014600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr17:20013400-20016000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr17:20013600-20014400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr17:20013600-20014400	Strong transcription	Aorta	Aorta
31	chr17:20013600-20014400	Strong transcription	Brain Inferior Temporal Lobe	brain
32	chr17:20013600-20014400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr17:20013600-20014400	Strong transcription	Ovary	ovary
34	chr17:20013600-20014600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr17:20013600-20016400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr17:20013800-20014000	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr17:20013800-20014000	Enhancers	Gastric	stomach
38	chr17:20013800-20014400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr17:20014000-20014400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr17:20014400-20019800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr17:20014400-20020000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr17:20014400-20024200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr17:20014400-20024400	Weak transcription	Ovary	ovary
44	chr17:20014400-20024800	Weak transcription	Aorta	Aorta
45	chr17:20014400-20025200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr17:20014600-20015200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr17:20014600-20028800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr17:20014800-20015200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr17:20015000-20015400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr17:20015000-20016400	Strong transcription	Adipose Nuclei	Adipose

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