Variant report

Variant	nsv902211
Chromosome Location	chr14:96864309-96986153
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1530)
CpG islands
(count:1525)
Chromatin interactive
region (count:106)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:96881799-96882325	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:96967807-96968858	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:96975227-96975533	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:96890757-96891051	K562	blood:	n/a	n/a
5	ARID3A	chr14:96973384-96973459	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:96890740-96891102	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:96928525-96928975	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:96876027-96876835	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:96978913-96979336	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:96935021-96935515	HepG2	liver:	n/a	n/a
11	ATF1	chr14:96882739-96882993	K562	blood:	n/a	n/a
12	ATF1	chr14:96968320-96968900	K562	blood:	n/a	chr14:96968699-96968713
13	ATF1	chr14:96908946-96909216	K562	blood:	n/a	n/a
14	ATF2	chr14:96968160-96968794	H1-hESC	embryonic stem cell:	n/a	chr14:96968699-96968713
15	ATF2	chr14:96968335-96968901	GM12878	blood:	n/a	chr14:96968699-96968713
16	ATF3	chr14:96928566-96928897	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr14:96928471-96929081	HepG2	liver:	n/a	n/a
18	BACH1	chr14:96968150-96968670	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr14:96908976-96909063	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr14:96969149-96969219	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr14:96968226-96968972	K562	blood:	n/a	n/a
22	BATF	chr14:96888445-96888712	GM12878	blood:	n/a	n/a
23	BATF	chr14:96888556-96888713	GM12878	blood:	n/a	n/a
24	BATF	chr14:96963428-96963708	GM12878	blood:	n/a	n/a
25	BCL3	chr14:96968052-96968938	A549	lung:	n/a	chr14:96968870-96968883 chr14:96968878-96968887 chr14:96968874-96968887 chr14:96968873-96968886 chr14:96968303-96968316 chr14:96968351-96968364 chr14:96968433-96968442
26	BCL3	chr14:96876155-96876393	GM12878	blood:	n/a	n/a
27	BCL3	chr14:96949985-96950252	GM12878	blood:	n/a	n/a
28	BCLAF1	chr14:96968913-96969704	GM12878	blood:	n/a	chr14:96969176-96969185
29	BCLAF1	chr14:96890757-96891003	GM12878	blood:	n/a	n/a
30	BCLAF1	chr14:96968123-96968997	GM12878	blood:	n/a	chr14:96968870-96968883 chr14:96968878-96968887 chr14:96968874-96968887 chr14:96968873-96968886 chr14:96968303-96968316 chr14:96968351-96968364 chr14:96968433-96968442
31	BCLAF1	chr14:96967906-96968878	GM12878	blood:	n/a	chr14:96968303-96968316 chr14:96968351-96968364 chr14:96968433-96968442
32	BHLHE40	chr14:96890822-96891035	K562	blood:	n/a	n/a
33	BHLHE40	chr14:96967868-96969564	K562	blood:	n/a	chr14:96969150-96969166 chr14:96969158-96969174
34	BHLHE40	chr14:96975974-96976436	GM12878	blood:	n/a	n/a
35	BHLHE40	chr14:96876101-96876287	HepG2	liver:	n/a	n/a
36	BHLHE40	chr14:96928490-96928949	HepG2	liver:	n/a	n/a
37	BHLHE40	chr14:96912602-96913014	K562	blood:	n/a	n/a
38	BHLHE40	chr14:96968130-96969386	GM12878	blood:	n/a	chr14:96969150-96969166 chr14:96969158-96969174
39	BHLHE40	chr14:96975224-96975384	HepG2	liver:	n/a	n/a
40	BHLHE40	chr14:96890785-96891084	GM12878	blood:	n/a	n/a
41	BHLHE40	chr14:96968192-96969199	HepG2	liver:	n/a	chr14:96969150-96969166 chr14:96969158-96969174
42	BHLHE40	chr14:96875010-96875175	HepG2	liver:	n/a	n/a
43	BRCA1	chr14:96968825-96969250	GM12878	blood:	n/a	n/a
44	BRCA1	chr14:96890817-96890939	GM12878	blood:	n/a	n/a
45	BRCA1	chr14:96968499-96968717	HepG2	liver:	n/a	n/a
46	BRCA1	chr14:96968258-96968734	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr14:96967961-96968840	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr14:96875936-96876544	HCT-116	colon:	n/a	n/a
49	CBX3	chr14:96968233-96968902	K562	blood:	n/a	n/a
50	CCNT2	chr14:96890506-96890725	K562	blood:	n/a	n/a

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:96967825-96967875	HRPEpiC	eye:	n/a
2	chr14:96887456-96887506	HAEpiC	amniotic membrane:	n/a
3	chr14:96965678-96965728	A549	lung:	n/a
4	chr14:96972280-96972330	AG09319	gingival:	n/a
5	chr14:96978537-96978587	SAEC	small airway:	n/a
6	chr14:96967798-96967848	GM12892	blood:	n/a
7	chr14:96968510-96968560	AG04450	lung:	fetal
8	chr14:96968737-96968787	BE2_C	brain:	n/a
9	chr14:96890632-96890682	SKMC	muscle:	n/a
10	chr14:96968625-96968675	K562	blood:	n/a
11	chr14:96967897-96967947	PFSK-1	brain:	n/a
12	chr14:96978537-96978587	HepG2	liver:	n/a
13	chr14:96967897-96967947	HCT-116	colon:	n/a
14	chr14:96890961-96891011	ovcar-3	ovarian:	n/a
15	chr14:96967897-96967947	SK-N-SH_RA	brain:	n/a
16	chr14:96890120-96890170	PANC-1	pancreas:	n/a
17	chr14:96955063-96955113	NH-A	brain:	n/a
18	chr14:96967897-96967947	Jurkat	blood:	n/a
19	chr14:96965678-96965728	HAEpiC	amniotic membrane:	n/a
20	chr14:96968050-96968100	HNPCEpiC	eye:	n/a
21	chr14:96893892-96893942	PrEC	prostate:	n/a
22	chr14:96965678-96965728	CMK	blood:	n/a
23	chr14:96968481-96968531	AG09319	gingival:	n/a
24	chr14:96978537-96978587	MCF10A-Er-Src	breast:	n/a
25	chr14:96969303-96969353	HAEpiC	amniotic membrane:	n/a
26	chr14:96972280-96972330	HPAEpiC	pulmonary alveolar:	n/a
27	chr14:96887456-96887506	HCM	heart:	n/a
28	chr14:96967798-96967848	PFSK-1	brain:	n/a
29	chr14:96968050-96968100	Jurkat	blood:	n/a
30	chr14:96890961-96891011	HepG2	liver:	n/a
31	chr14:96955063-96955113	MCF10A-Er-Src	breast:	n/a
32	chr14:96968050-96968100	CMK	blood:	n/a
33	chr14:96955063-96955113	HIPEpiC	eye:	n/a
34	chr14:96969243-96969293	HEEpiC	esophagus:	n/a
35	chr14:96965678-96965728	U87	brain:	n/a
36	chr14:96968050-96968100	AG04449	skin:	fetal
37	chr14:96968625-96968675	PrEC	prostate:	n/a
38	chr14:96968481-96968531	GM19239	blood:	n/a
39	chr14:96967798-96967848	GM06990	blood:	n/a
40	chr14:96890961-96891011	HCT-116	colon:	n/a
41	chr14:96972280-96972330	NH-A	brain:	n/a
42	chr14:96968510-96968560	NH-A	brain:	n/a
43	chr14:96967798-96967848	LNCaP	prostate:	n/a
44	chr14:96970127-96970177	HNPCEpiC	eye:	n/a
45	chr14:96890449-96890499	RPTEC	kidney:	n/a
46	chr14:96967897-96967947	HEK293	kidney:	embryo
47	chr14:96955063-96955113	AG04449	skin:	fetal
48	chr14:96968481-96968531	T-47D	breast:	n/a
49	chr14:96890120-96890170	HCM	heart:	n/a
50	chr14:96978537-96978587	BE2_C	brain:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:96968120..96968788-chr17:80250092..80250824,2	Hela-S3	cervix:
2	chr10:5854507..5855433-chr14:96968652..96969152,2	Hela-S3	cervix:
3	chr14:96977217..96979586-chr14:96982926..96984761,2	MCF-7	breast:
4	chr14:96946909..96948979-chr14:96949809..96951767,2	MCF-7	breast:
5	chr14:96985630..96987652-chr14:97013134..97015914,2	MCF-7	breast:
6	chr14:96866375..96868944-chr14:96869900..96872198,3	K562	blood:
7	chr14:96889980..96892782-chr14:96967434..96969470,2	MCF-7	breast:
8	chr14:96856592..96858411-chr14:96867696..96870536,2	K562	blood:
9	chr14:96973732..96976070-chr14:96984297..96985956,2	K562	blood:
10	chr14:96944597..96947618-chr14:96962282..96964814,3	MCF-7	breast:
11	chr14:96977217..96979586-chr14:96982926..96984761,2	MCF-7	breast:
12	chr14:96958156..96960045-chr14:96966380..96969772,3	MCF-7	breast:
13	chr14:96759438..96761870-chr14:96967375..96970054,2	MCF-7	breast:
14	chr14:96928829..96930351-chr14:96930416..96933252,2	MCF-7	breast:
15	chr14:96967956..96970809-chr14:96981741..96983595,3	MCF-7	breast:
16	chr14:96967861..96968445-chr20:47662706..47663268,2	Hela-S3	cervix:
17	chr14:96918260..96919930-chr14:96921277..96923704,2	MCF-7	breast:
18	chr14:96913037..96914989-chr14:96966222..96968484,2	MCF-7	breast:
19	chr14:96907078..96909690-chr14:96925295..96927351,2	K562	blood:
20	chr14:96967969..96968570-chr17:48943455..48944322,2	Hela-S3	cervix:
21	chr14:96856306..96858338-chr14:96865054..96868608,3	MCF-7	breast:
22	chr14:96950411..96952541-chr14:96959008..96961670,2	MCF-7	breast:
23	chr14:96870571..96872303-chr14:96873260..96875995,2	K562	blood:
24	chr14:96866348..96868944-chr14:96869498..96872110,3	K562	blood:
25	chr14:96968426..96968992-chr19:9731602..9732102,2	NB4	blood:
26	chr14:96903862..96905382-chr4:37697642..37700393,2	K562	blood:
27	chr14:96950411..96952541-chr14:96959008..96961670,2	MCF-7	breast:
28	chr14:96975313..96976857-chr14:96978601..96981439,2	MCF-7	breast:
29	chr14:96828603..96830880-chr14:96964867..96966868,2	MCF-7	breast:
30	chr1:151512325..151513409-chr14:96967489..96968213,3	Hela-S3	cervix:
31	chr14:96876815..96879566-chr14:96880954..96883744,3	K562	blood:
32	chr14:96967942..96968907-chr16:2014395..2014982,2	Hela-S3	cervix:
33	chr14:96953364..96956341-chr14:96967699..96969947,2	K562	blood:
34	chr14:96928829..96930351-chr14:96930416..96933252,2	MCF-7	breast:
35	chr14:96824632..96827267-chr14:96972048..96974054,2	K562	blood:
36	chr14:96207305..96209332-chr14:96958131..96960093,2	MCF-7	breast:
37	chr14:96866375..96868944-chr14:96869900..96872198,3	K562	blood:
38	chr14:96960614..96962618-chr14:96966589..96970350,3	K562	blood:
39	chr14:96980357..96982346-chr14:96989639..96991890,2	MCF-7	breast:
40	chr14:96871974..96874512-chr14:96876707..96880764,3	K562	blood:
41	chr1:46216043..46216614-chr14:96968529..96969256,2	Hela-S3	cervix:
42	chr14:96862007..96865394-chr14:96865688..96870524,5	MCF-7	breast:
43	chr14:96926645..96928449-chr14:96967530..96969889,2	MCF-7	breast:
44	chr14:96900159..96902120-chr14:96968075..96970650,2	MCF-7	breast:
45	chr14:96789748..96793342-chr14:96967409..96970462,3	K562	blood:
46	chr14:96967956..96969589-chr9:140512244..140513858,2	MCF-7	breast:
47	chr1:110950294..110950915-chr14:96968126..96968634,2	Hela-S3	cervix:
48	chr14:96870571..96872303-chr14:96873260..96875995,2	K562	blood:
49	chr14:96909028..96911274-chr14:96967250..96968928,2	MCF-7	breast:
50	chr14:96916163..96917945-chr14:96968415..96970452,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG2B-2	chr14:96967985-96968630	NONHSAT039531
2	lnc-ATG2B-2	chr14:96967147-96968658	ENSG00000260806.1
3	lnc-ATG2B-1	chr14:96932561-96932661	ENSG00000258530.1
4	lnc-PAPOLA-3	chr14:96949043-96949280	uc_381_+
5	lnc-ATG2B-7	chr14:96949043-96949280	uc_381_-
6	lnc-ATG2B-6	chr14:96922913-96923378	NONHSAT039527
7	lnc-ATG2B-1	chr14:96939596-96940208	ENSG00000258530.1
8	lnc-ATG2B-2	chr14:96967028-96968641	NONHSAT039529

No data

Variant related genes	Relation type
PAPOLA	TF binding region
RPL23AP10	TF binding region
ENSG00000260806	TF binding region
AK7	TF binding region
PEBP1P1	TF binding region
PAPOLA	CpG island
RPL23AP10	CpG island
ENSG00000260806	CpG island
AK7	CpG island
PEBP1P1	CpG island
ENSG00000134248	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000168395	chromatin interactions
ENSG00000173207	chromatin interactions
ENSG00000188693	chromatin interactions
ENSG00000267106	chromatin interactions
ENSG00000066739	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000259059	chromatin interactions
ENSG00000255198	chromatin interactions
ENSG00000224699	chromatin interactions
ENSG00000229980	chromatin interactions
ENSG00000140988	chromatin interactions
ENSG00000197429	chromatin interactions
ENSG00000235706	chromatin interactions
ENSG00000057608	chromatin interactions
ENSG00000170315	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000171469	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000265692	chromatin interactions
ENSG00000086758	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000238776	chromatin interactions
ENSG00000160691	chromatin interactions
ENSG00000122034	chromatin interactions
ENSG00000124207	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000167930	chromatin interactions
ENSG00000260806	chromatin interactions
ENSG00000228265	chromatin interactions
ENSG00000100697	chromatin interactions
ENSG00000125970	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000105323	chromatin interactions
ENSG00000145740	chromatin interactions
ENSG00000140057	chromatin interactions
ENSG00000100744	chromatin interactions
ENSG00000001630	chromatin interactions
ENSG00000240051	chromatin interactions

Extended variants
information (count: 4479 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4479 , 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	rs8019939	chr14:96864309-96864310	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs41301765	chr14:96864327-96864328	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs566558931	chr14:96864346-96864347	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371239182	chr14:96864361-96864362	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs374779639	chr14:96864364-96864365	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368518247	chr14:96864366-96864367	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs41317306	chr14:96864374-96864375	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375973401	chr14:96864384-96864385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187794852	chr14:96864387-96864388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs193004081	chr14:96864398-96864399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs140159462	chr14:96864441-96864442	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200321438	chr14:96864462-96864463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs115324937	chr14:96864504-96864505	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs151078589	chr14:96864511-96864512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs17853407	chr14:96864516-96864517	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs117932049	chr14:96864529-96864530	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs202102376	chr14:96864531-96864532	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs140870082	chr14:96864548-96864549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs373215673	chr14:96864570-96864571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs199700054	chr14:96864571-96864572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs115194868	chr14:96864574-96864575	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs543208617	chr14:96864579-96864580	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs114723307	chr14:96864585-96864586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs376030667	chr14:96864591-96864592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs529120178	chr14:96864614-96864615	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs540913912	chr14:96864636-96864637	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369245246	chr14:96864637-96864638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs370340365	chr14:96864652-96864653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs527666689	chr14:96864653-96864654	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141289669	chr14:96864654-96864655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs183745851	chr14:96864661-96864662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544713251	chr14:96864675-96864676	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs115678716	chr14:96864688-96864689	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs550071037	chr14:96864726-96864727	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146556378	chr14:96864767-96864768	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs564954184	chr14:96864782-96864783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139112163	chr14:96864786-96864787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554503753	chr14:96864808-96864809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs545015123	chr14:96864834-96864835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148932970	chr14:96864853-96864854	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188414017	chr14:96864884-96864885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143647525	chr14:96864895-96864896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs73349240	chr14:96864899-96864900	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543522660	chr14:96864923-96864924	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530670642	chr14:96864925-96864926	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555208868	chr14:96864928-96864929	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564810041	chr14:96864944-96864945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570470745	chr14:96864947-96864948	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540864885	chr14:96864970-96864971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs192444322	chr14:96865030-96865031	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Glioblastoma	21080181	CNVD
Cancer	20164920	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Breast cancer	21509527	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1876 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:96859000-96866600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr14:96859000-96874400	Weak transcription	Spleen	Spleen
3	chr14:96859000-96890400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr14:96859400-96865800	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr14:96859400-96865800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr14:96859400-96866600	Weak transcription	Brain Anterior Caudate	brain
7	chr14:96859800-96869800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr14:96863400-96878000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:96864600-96864800	Enhancers	K562	blood
10	chr14:96865800-96866000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr14:96865800-96866000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr14:96866000-96886400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:96866600-96867200	Enhancers	Brain Hippocampus Middle	brain
14	chr14:96866600-96867400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr14:96866600-96867600	Enhancers	Brain Anterior Caudate	brain
16	chr14:96866600-96867600	Enhancers	Brain Cingulate Gyrus	brain
17	chr14:96866800-96867200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
18	chr14:96866800-96867600	Enhancers	Brain Angular Gyrus	brain
19	chr14:96866800-96867600	Enhancers	Brain Substantia Nigra	brain
20	chr14:96866800-96867800	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr14:96867200-96867400	Flanking Active TSS	Brain Hippocampus Middle	brain
22	chr14:96867400-96867600	Enhancers	Brain Hippocampus Middle	brain
23	chr14:96867600-96879600	Weak transcription	Brain Anterior Caudate	brain
24	chr14:96867600-96881600	Weak transcription	Brain Substantia Nigra	brain
25	chr14:96868000-96876000	Weak transcription	Pancreas	Pancrea
26	chr14:96869600-96869800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr14:96869600-96869800	Enhancers	Left Ventricle	heart
28	chr14:96869600-96870000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:96869600-96870200	Enhancers	HUVEC	blood vessel
30	chr14:96869600-96870400	Enhancers	Lung	lung
31	chr14:96869800-96870000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr14:96870000-96872000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr14:96870000-96872400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr14:96870400-96874400	Weak transcription	Lung	lung
35	chr14:96871000-96872800	Enhancers	K562	blood
36	chr14:96871600-96871800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr14:96871800-96872800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:96872000-96872400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr14:96872400-96872600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr14:96872400-96872800	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr14:96872400-96872800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:96872400-96876000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr14:96872600-96872800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr14:96872800-96873200	Enhancers	Primary hematopoietic stem cells	blood
45	chr14:96872800-96874000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr14:96872800-96874200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr14:96872800-96874200	Weak transcription	K562	blood
48	chr14:96873200-96874200	Weak transcription	Primary hematopoietic stem cells	blood
49	chr14:96873400-96874400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:96874200-96874600	Flanking Active TSS	K562	blood

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