Variant report

Variant	nsv832763
Chromosome Location	chr14:31501597-31680021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3188)
CpG islands
(count:1162)
Chromatin interactive
region (count:156)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3188 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:31507773-31508345	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:31674388-31675448	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:31561638-31561823	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:31573701-31573703	K562	blood:	n/a	n/a
5	ARID3A	chr14:31549348-31549622	K562	blood:	n/a	n/a
6	ARID3A	chr14:31676703-31678030	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:31507099-31507550	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:31667026-31667216	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:31511604-31511770	K562	blood:	n/a	n/a
10	ARID3A	chr14:31522527-31522614	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:31524101-31524173	K562	blood:	n/a	n/a
12	ARID3A	chr14:31528245-31529150	K562	blood:	n/a	n/a
13	ARID3A	chr14:31596940-31597257	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:31501593-31501611	K562	blood:	n/a	n/a
15	ARID3A	chr14:31551219-31551628	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:31502435-31503536	HepG2	liver:	n/a	n/a
17	ARID3A	chr14:31633342-31633560	HepG2	liver:	n/a	n/a
18	ARID3A	chr14:31551258-31551518	K562	blood:	n/a	n/a
19	ARID3A	chr14:31559886-31561386	HepG2	liver:	n/a	n/a
20	ARID3A	chr14:31507685-31508382	K562	blood:	n/a	n/a
21	ARID3A	chr14:31676990-31677431	K562	blood:	n/a	n/a
22	ARID3A	chr14:31669217-31669582	K562	blood:	n/a	n/a
23	ATF1	chr14:31507743-31508407	K562	blood:	n/a	n/a
24	ATF1	chr14:31517729-31518127	K562	blood:	n/a	n/a
25	ATF1	chr14:31669163-31669692	K562	blood:	n/a	n/a
26	ATF1	chr14:31560047-31560326	K562	blood:	n/a	n/a
27	ATF1	chr14:31677060-31677669	K562	blood:	n/a	n/a
28	ATF1	chr14:31528770-31529181	K562	blood:	n/a	n/a
29	ATF2	chr14:31502127-31502530	GM12878	blood:	n/a	n/a
30	ATF2	chr14:31677042-31678003	GM12878	blood:	n/a	n/a
31	ATF2	chr14:31676407-31678063	GM12878	blood:	n/a	n/a
32	ATF2	chr14:31501963-31502660	GM12878	blood:	n/a	n/a
33	ATF3	chr14:31517648-31518167	HCT-116	colon:	n/a	n/a
34	ATF3	chr14:31676915-31677439	A549	lung:	n/a	n/a
35	ATF3	chr14:31517760-31518091	K562	blood:	n/a	n/a
36	ATF3	chr14:31528688-31529112	K562	blood:	n/a	n/a
37	ATF3	chr14:31677261-31677456	K562	blood:	n/a	n/a
38	ATF3	chr14:31507734-31508127	K562	blood:	n/a	n/a
39	ATF3	chr14:31676703-31677570	HepG2	liver:	n/a	n/a
40	BACH1	chr14:31551367-31551442	K562	blood:	n/a	n/a
41	BACH1	chr14:31676759-31677544	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr14:31677868-31678382	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr14:31677838-31678318	K562	blood:	n/a	n/a
44	BACH1	chr14:31551362-31551542	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr14:31528791-31529048	K562	blood:	n/a	n/a
46	BATF	chr14:31675862-31676128	GM12878	blood:	n/a	n/a
47	BATF	chr14:31674187-31674369	GM12878	blood:	n/a	n/a
48	BATF	chr14:31674199-31674376	GM12878	blood:	n/a	n/a
49	BATF	chr14:31502184-31502487	GM12878	blood:	n/a	n/a
50	BATF	chr14:31676959-31677963	GM12878	blood:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31675363-31675413	NHBE	bronchial:	n/a
2	chr14:31673220-31673270	HPAEpiC	pulmonary alveolar:	n/a
3	chr14:31607371-31607421	NHDF-neo	bronchial:	n/a
4	chr14:31675363-31675413	NHBE	bronchial:	n/a
5	chr14:31673220-31673270	HPAEpiC	pulmonary alveolar:	n/a
6	chr14:31607371-31607421	NHDF-neo	bronchial:	n/a
7	chr14:31549691-31549741	HCF	heart:	n/a
8	chr14:31673220-31673270	PFSK-1	brain:	n/a
9	chr14:31677445-31677495	LNCaP	prostate:	n/a
10	chr14:31560529-31560579	HepG2	liver:	n/a
11	chr14:31675363-31675413	GM12878	blood:	n/a
12	chr14:31562255-31562305	AG04450	lung:	fetal
13	chr14:31677288-31677338	NH-A	brain:	n/a
14	chr14:31677716-31677766	HIPEpiC	eye:	n/a
15	chr14:31675363-31675413	SK-N-SH_RA	brain:	n/a
16	chr14:31529383-31529433	PANC-1	pancreas:	n/a
17	chr14:31676815-31676865	NHBE	bronchial:	n/a
18	chr14:31677607-31677657	Caco-2	colon:	n/a
19	chr14:31560529-31560579	AG04449	skin:	fetal
20	chr14:31673220-31673270	HL-60	blood:	n/a
21	chr14:31676811-31676861	HIPEpiC	eye:	n/a
22	chr14:31549691-31549741	RPTEC	kidney:	n/a
23	chr14:31677219-31677269	PrEC	prostate:	n/a
24	chr14:31529383-31529433	CMK	blood:	n/a
25	chr14:31529383-31529433	Jurkat	blood:	n/a
26	chr14:31677607-31677657	CMK	blood:	n/a
27	chr14:31676815-31676865	HCM	heart:	n/a
28	chr14:31679612-31679662	HUVEC	blood vessel:	n/a
29	chr14:31554343-31554393	Jurkat	blood:	n/a
30	chr14:31676328-31676378	Hepatocyte	liver:	n/a
31	chr14:31677445-31677495	HRCEpiC	kidney:	n/a
32	chr14:31676328-31676378	MCF-7	breast:	n/a
33	chr14:31677445-31677495	HCPEpiC	choroid plexus:	n/a
34	chr14:31676811-31676861	AG04449	skin:	fetal
35	chr14:31673220-31673270	SK-N-SH	brain:	n/a
36	chr14:31677607-31677657	HIPEpiC	eye:	n/a
37	chr14:31560529-31560579	Caco-2	colon:	n/a
38	chr14:31549691-31549741	IMR90	lung:	fetal
39	chr14:31677445-31677495	AG04449	skin:	fetal
40	chr14:31676207-31676257	HUVEC	blood vessel:	n/a
41	chr14:31677716-31677766	SAEC	small airway:	n/a
42	chr14:31677445-31677495	NHDF-neo	bronchial:	n/a
43	chr14:31676328-31676378	K562	blood:	n/a
44	chr14:31675363-31675413	Hepatocyte	liver:	n/a
45	chr14:31507716-31507766	BJ	skin:	n/a
46	chr14:31676207-31676257	T-47D	breast:	n/a
47	chr14:31677219-31677269	A549	lung:	n/a
48	chr14:31507716-31507766	A549	lung:	n/a
49	chr14:31679612-31679662	Hela-S3	cervix:	n/a
50	chr14:31562255-31562305	AG09309	skin:	n/a

(count:156 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr14:31494053..31496608-chr14:31524504..31526013,2	K562	blood:
2	chr14:31676028..31679220-chr14:31679560..31682621,5	MCF-7	breast:
3	chr14:31675912..31678861-chr14:31887650..31889789,3	K562	blood:
4	chr14:31535994..31538827-chr14:31544129..31546661,2	K562	blood:
5	chr14:31566343..31568008-chr14:31570057..31571588,2	K562	blood:
6	chr14:31646873..31649648-chr14:31650062..31652534,2	MCF-7	breast:
7	chr14:31677416..31678964-chr14:31720140..31723072,2	K562	blood:
8	chr14:31633500..31636890-chr14:31639445..31642730,4	MCF-7	breast:
9	chr14:31493158..31494786-chr14:31553832..31556036,2	K562	blood:
10	chr14:31545887..31548153-chr14:31549801..31551382,2	K562	blood:
11	chr14:31677211..31678076-chr4:156681705..156682534,2	MCF-7	breast:
12	chr14:31500890..31503560-chr14:31504329..31508150,5	K562	blood:
13	chr14:31077974..31078580-chr14:31550888..31551785,2	K562	blood:
14	chr14:31654015..31656848-chr14:31657830..31660066,3	K562	blood:
15	chr14:31529023..31531109-chr14:31534744..31536932,2	K562	blood:
16	chr14:31494054..31496618-chr14:31538814..31541069,2	MCF-7	breast:
17	chr14:31495964..31498060-chr14:31518106..31520616,2	MCF-7	breast:
18	chr14:31601205..31602720-chr14:31611086..31613417,2	MCF-7	breast:
19	chr14:31548388..31550747-chr14:31553010..31555958,3	K562	blood:
20	chr14:31493836..31495813-chr14:31549240..31552533,4	MCF-7	breast:
21	chr14:31494347..31495920-chr14:31544461..31546849,2	MCF-7	breast:
22	chr14:31662501..31665350-chr14:31676259..31678758,2	MCF-7	breast:
23	chr14:31344003..31345728-chr14:31604211..31605992,2	K562	blood:
24	chr14:31634801..31637457-chr14:31677237..31679134,2	K562	blood:
25	chr14:31677147..31677806-chr7:77167282..77168042,2	NB4	blood:
26	chr14:31495016..31496980-chr14:31552994..31555861,2	MCF-7	breast:
27	chr14:31661874..31669449-chr14:31675207..31678992,11	MCF-7	breast:
28	chr14:31676619..31677277-chr14:31889333..31889964,2	K562	blood:
29	chr14:31677147..31678003-chr2:85765862..85766503,2	NB4	blood:
30	chr14:31592934..31595654-chr14:31599577..31602427,2	MCF-7	breast:
31	chr13:41635261..41636148-chr14:31676476..31676985,2	HCT-116	colon:
32	chr14:31676195..31678341-chr2:204101427..204103984,2	MCF-7	breast:
33	chr14:31560677..31562570-chr14:31676367..31678579,2	MCF-7	breast:
34	chr14:31676795..31677350-chr16:21610177..21611094,2	Hela-S3	cervix:
35	chr14:31633500..31636890-chr14:31639445..31642730,4	MCF-7	breast:
36	chr14:31648055..31651023-chr14:31675451..31677498,2	MCF-7	breast:
37	chr14:31493804..31495692-chr14:31511099..31513594,2	MCF-7	breast:
38	chr14:31662672..31665414-chr14:31666096..31668689,4	K562	blood:
39	chr1:150534629..150535612-chr14:31677743..31678393,2	Hela-S3	cervix:
40	chr14:31471923..31474357-chr14:31505063..31507952,2	K562	blood:
41	chr14:31666318..31667928-chr14:31887002..31889719,2	K562	blood:
42	chr14:31667035..31669074-chr14:31688594..31690835,2	K562	blood:
43	chr14:31676908..31677885-chr20:25604560..25605123,2	Hela-S3	cervix:
44	chr14:31676274..31678860-chr14:31889133..31891124,4	MCF-7	breast:
45	chr14:31500766..31503051-chr14:31511227..31514419,3	MCF-7	breast:
46	chr14:31507963..31510903-chr14:31527349..31529019,3	K562	blood:
47	chr14:31641311..31643841-chr14:31675872..31678556,3	MCF-7	breast:
48	chr14:31592934..31595654-chr14:31599577..31602427,2	MCF-7	breast:
49	chr14:31677392..31679217-chr14:31684991..31686865,2	MCF-7	breast:
50	chr14:31592178..31594075-chr14:31598650..31601042,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STRN3-5	chr14:31581213-31581445	NONHSAT036266
2	lnc-STRN3-11	chr14:31614377-31615656	l_960_NR_027263
3	lnc-STRN3-5	chr14:31580775-31581013	NONHSAT036266

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AP4S1	hsa-miR-15b-5p	chr14:31554320-31554342

Variant related genes	Relation type
RPL21P5	TF binding region
RNU6-541P	TF binding region
AP4S1	TF binding region
HECTD1	TF binding region
RPL21P5	CpG island
RNU6-541P	CpG island
AP4S1	CpG island
HECTD1	CpG island
ENSG00000075413	chromatin interactions
ENSG00000129493	chromatin interactions
ENSG00000197006	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000119004	chromatin interactions
ENSG00000207440	chromatin interactions
ENSG00000120690	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000213742	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000135119	chromatin interactions
ENSG00000111412	chromatin interactions
ENSG00000127947	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000129480	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000264395	chromatin interactions
ENSG00000120688	chromatin interactions
ENSG00000258640	chromatin interactions

Extended variants
information (count: 6932 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:6932 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28399181	chr14:31501609-31501610	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs541667798	chr14:31501743-31501744	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs10687883	chr14:31501744-31501745	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs188274055	chr14:31501814-31501815	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs150832293	chr14:31501877-31501878	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs139298611	chr14:31501895-31501896	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs193284165	chr14:31501902-31501903	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs61976819	chr14:31501903-31501904	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533206421	chr14:31501923-31501924	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs34527888	chr14:31501933-31501934	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs566726231	chr14:31501956-31501957	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs141324593	chr14:31501966-31501967	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs143807117	chr14:31501968-31501969	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568468192	chr14:31501977-31501978	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs145848124	chr14:31501982-31501983	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541424256	chr14:31502045-31502046	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs574990449	chr14:31502152-31502153	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs557072796	chr14:31502213-31502214	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs201537379	chr14:31502242-31502243	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185494803	chr14:31502256-31502257	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs545942865	chr14:31502311-31502312	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs186800229	chr14:31502318-31502319	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573422501	chr14:31502342-31502343	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs372489315	chr14:31502450-31502451	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs540941497	chr14:31502451-31502452	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs3784157	chr14:31502459-31502460	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs528920062	chr14:31502480-31502481	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs143014046	chr14:31502481-31502482	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs191272626	chr14:31502489-31502490	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs115964382	chr14:31502540-31502541	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs551562500	chr14:31502550-31502551	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs368849092	chr14:31502610-31502611	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs560405106	chr14:31502611-31502612	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs3784158	chr14:31502636-31502637	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs549292632	chr14:31502637-31502638	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs146945493	chr14:31502646-31502647	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs535890049	chr14:31502650-31502651	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs3784159	chr14:31502651-31502652	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs2064824	chr14:31502665-31502666	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs188577440	chr14:31502686-31502687	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539559495	chr14:31502697-31502698	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs557900612	chr14:31502701-31502702	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573411723	chr14:31502702-31502703	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs534212352	chr14:31502705-31502706	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs556068940	chr14:31502707-31502708	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs376006730	chr14:31502709-31502710	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs573556152	chr14:31502710-31502711	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs544180420	chr14:31502714-31502715	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562477620	chr14:31502797-31502798	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs76919081	chr14:31502812-31502813	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4918 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31496600-31505800	Weak transcription	Primary T cells from cord blood	blood
2	chr14:31496600-31507800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr14:31496600-31509800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr14:31496600-31515800	Weak transcription	Thymus	Thymus
5	chr14:31496800-31501800	Weak transcription	Pancreas	Pancrea
6	chr14:31496800-31502400	Weak transcription	Ovary	ovary
7	chr14:31496800-31505800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr14:31496800-31507000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr14:31496800-31507600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr14:31496800-31508400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr14:31496800-31508600	Weak transcription	Lung	lung
12	chr14:31496800-31511200	Weak transcription	Brain Anterior Caudate	brain
13	chr14:31496800-31517600	Weak transcription	Left Ventricle	heart
14	chr14:31496800-31517800	Weak transcription	Brain Hippocampus Middle	brain
15	chr14:31496800-31517800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr14:31496800-31522400	Weak transcription	Right Atrium	heart
17	chr14:31496800-31527600	Weak transcription	Primary B cells from peripheral blood	blood
18	chr14:31497000-31501600	Weak transcription	Liver	Liver
19	chr14:31497000-31502000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr14:31497000-31502000	Weak transcription	HSMM	muscle
21	chr14:31497000-31502200	Weak transcription	Fetal Muscle Leg	muscle
22	chr14:31497000-31502400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr14:31497000-31502400	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr14:31497000-31502600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr14:31497000-31502800	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr14:31497000-31505800	Weak transcription	Fetal Stomach	stomach
27	chr14:31497000-31506200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr14:31497000-31506400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr14:31497000-31507600	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr14:31497000-31508800	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr14:31497000-31512200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr14:31497000-31512200	Weak transcription	Psoas Muscle	Psoas
33	chr14:31497000-31568600	Weak transcription	Fetal Kidney	kidney
34	chr14:31497200-31502000	Enhancers	HepG2	liver
35	chr14:31497200-31502200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr14:31497200-31502600	Weak transcription	Osteobl	bone
37	chr14:31497200-31509200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr14:31497400-31512400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr14:31497600-31502200	Weak transcription	Duodenum Mucosa	Duodenum
40	chr14:31497600-31502400	Weak transcription	Fetal Intestine Large	intestine
41	chr14:31497600-31502800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr14:31497600-31502800	Weak transcription	NHDF-Ad	bronchial
43	chr14:31497600-31507200	Weak transcription	Fetal Intestine Small	intestine
44	chr14:31497600-31552800	Weak transcription	Fetal Muscle Trunk	muscle
45	chr14:31500000-31504200	Enhancers	Hela-S3	cervix
46	chr14:31500400-31503600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr14:31500400-31503800	Enhancers	HMEC	breast
48	chr14:31500600-31501600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr14:31500600-31503800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr14:31500800-31501800	Flanking Active TSS	K562	blood

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