Variant report

Variant	nsv1050597
Chromosome Location	chr14:31711248-31904761
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3185)
CpG islands
(count:915)
Chromatin interactive
region (count:103)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:3185 , 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	chr14:31749636-31749982	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:31756012-31756205	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:31889740-31890190	K562	blood:	n/a	n/a
4	ARID3A	chr14:31847057-31847719	HepG2	liver:	n/a	chr14:31847087-31847103
5	ARID3A	chr14:31888898-31891391	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:31824941-31825507	HepG2	liver:	n/a	chr14:31825219-31825235
7	ARID3A	chr14:31760525-31760637	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:31731165-31731697	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:31732875-31734007	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:31902751-31902786	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:31825017-31825479	K562	blood:	n/a	chr14:31825219-31825235
12	ARID3A	chr14:31820348-31820569	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:31735125-31735523	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:31735146-31735170	K562	blood:	n/a	n/a
15	ARID3A	chr14:31805945-31806204	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:31752861-31752917	HepG2	liver:	n/a	n/a
17	ARID3A	chr14:31727109-31727795	HepG2	liver:	n/a	n/a
18	ARID3A	chr14:31745094-31745146	HepG2	liver:	n/a	n/a
19	ATF1	chr14:31847379-31847549	K562	blood:	n/a	n/a
20	ATF1	chr14:31713059-31713378	K562	blood:	n/a	n/a
21	ATF1	chr14:31711643-31711937	K562	blood:	n/a	n/a
22	ATF1	chr14:31875168-31875448	K562	blood:	n/a	n/a
23	ATF2	chr14:31889628-31890309	GM12878	blood:	n/a	n/a
24	ATF2	chr14:31889508-31890142	GM12878	blood:	n/a	n/a
25	ATF2	chr14:31752743-31753207	GM12878	blood:	n/a	n/a
26	ATF2	chr14:31739301-31739683	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr14:31739320-31739669	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF3	chr14:31875173-31875422	K562	blood:	n/a	n/a
29	ATF3	chr14:31889517-31890325	A549	lung:	n/a	n/a
30	BACH1	chr14:31825281-31825293	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr14:31889072-31890103	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr14:31893454-31893489	K562	blood:	n/a	n/a
33	BACH1	chr14:31734997-31735181	K562	blood:	n/a	n/a
34	BACH1	chr14:31713147-31713431	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr14:31713253-31713448	GM12878	blood:	n/a	chr14:31713355-31713366 chr14:31713380-31713391
36	BATF	chr14:31890090-31890408	GM12878	blood:	n/a	n/a
37	BATF	chr14:31767205-31767473	GM12878	blood:	n/a	n/a
38	BATF	chr14:31743100-31743464	GM12878	blood:	n/a	chr14:31743263-31743274
39	BATF	chr14:31857940-31858574	GM12878	blood:	n/a	chr14:31858232-31858243
40	BATF	chr14:31726501-31726801	GM12878	blood:	n/a	n/a
41	BATF	chr14:31733444-31733742	GM12878	blood:	n/a	n/a
42	BATF	chr14:31752796-31753085	GM12878	blood:	n/a	n/a
43	BATF	chr14:31733446-31733788	GM12878	blood:	n/a	n/a
44	BATF	chr14:31743102-31743470	GM12878	blood:	n/a	chr14:31743263-31743274
45	BATF	chr14:31767240-31767482	GM12878	blood:	n/a	n/a
46	BCL11A	chr14:31887740-31887953	GM12878	blood:	n/a	n/a
47	BCL3	chr14:31889359-31890148	A549	lung:	n/a	chr14:31889766-31889779
48	BCLAF1	chr14:31889496-31890203	GM12878	blood:	n/a	chr14:31889766-31889779
49	BHLHE40	chr14:31889290-31890317	K562	blood:	n/a	n/a
50	BHLHE40	chr14:31879528-31879697	GM12878	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31859505-31859555	HRE	kidney:	n/a
2	chr14:31762081-31762131	HMEC	breast:	n/a
3	chr14:31886488-31886538	HUVEC	blood vessel:	n/a
4	chr14:31889640-31889690	AG09309	skin:	n/a
5	chr14:31859515-31859565	U87	brain:	n/a
6	chr14:31886488-31886538	PrEC	prostate:	n/a
7	chr14:31858067-31858117	HNPCEpiC	eye:	n/a
8	chr14:31889169-31889219	AG10803	skin:	n/a
9	chr14:31731725-31731775	HMEC	breast:	n/a
10	chr14:31889003-31889053	AG04449	skin:	fetal
11	chr14:31859515-31859565	HRCEpiC	kidney:	n/a
12	chr14:31858202-31858252	HCPEpiC	choroid plexus:	n/a
13	chr14:31858202-31858252	HRCEpiC	kidney:	n/a
14	chr14:31889169-31889219	BE2_C	brain:	n/a
15	chr14:31890052-31890102	ProgFib	skin:	n/a
16	chr14:31889640-31889690	ECC-1	luminal epithelium:	n/a
17	chr14:31859505-31859555	SKMC	muscle:	n/a
18	chr14:31892296-31892346	T-47D	breast:	n/a
19	chr14:31858067-31858117	Jurkat	blood:	n/a
20	chr14:31889640-31889690	NHBE	bronchial:	n/a
21	chr14:31889169-31889219	NHBE	bronchial:	n/a
22	chr14:31889003-31889053	NB4	blood:	n/a
23	chr14:31859515-31859565	HCT-116	colon:	n/a
24	chr14:31731725-31731775	AoSMC	blood vessel:	n/a
25	chr14:31762081-31762131	AG04449	skin:	fetal
26	chr14:31890052-31890102	NHDF-neo	bronchial:	n/a
27	chr14:31892296-31892346	SK-N-SH_RA	brain:	n/a
28	chr14:31858067-31858117	A549	lung:	n/a
29	chr14:31731725-31731775	Hepatocyte	liver:	n/a
30	chr14:31858067-31858117	MCF10A-Er-Src	breast:	n/a
31	chr14:31859505-31859555	T-47D	breast:	n/a
32	chr14:31886488-31886538	NT2-D1	testis:	n/a
33	chr14:31892296-31892346	MCF10A-Er-Src	breast:	n/a
34	chr14:31764703-31764753	PFSK-1	brain:	n/a
35	chr14:31731725-31731775	GM12891	blood:	n/a
36	chr14:31889640-31889690	AG04450	lung:	fetal
37	chr14:31886488-31886538	AoSMC	blood vessel:	n/a
38	chr14:31764703-31764753	HL-60	blood:	n/a
39	chr14:31731725-31731775	HNPCEpiC	eye:	n/a
40	chr14:31889912-31889962	A549	lung:	n/a
41	chr14:31890001-31890051	SK-N-SH	brain:	n/a
42	chr14:31859515-31859565	SAEC	small airway:	n/a
43	chr14:31889640-31889690	HEEpiC	esophagus:	n/a
44	chr14:31892296-31892346	HCPEpiC	choroid plexus:	n/a
45	chr14:31858202-31858252	AG04449	skin:	fetal
46	chr14:31889003-31889053	AoSMC	blood vessel:	n/a
47	chr14:31889640-31889690	HCF	heart:	n/a
48	chr14:31889912-31889962	RPTEC	kidney:	n/a
49	chr14:31731725-31731775	HPAEpiC	pulmonary alveolar:	n/a
50	chr14:31764703-31764753	SAEC	small airway:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:31727752..31730526-chr14:31730596..31732491,2	K562	blood:
2	chr14:31721356..31723152-chr14:31729738..31731709,2	MCF-7	breast:
3	chr14:31676075..31678672-chr14:31762888..31766757,3	MCF-7	breast:
4	chr14:31863925..31866635-chr14:31868935..31870560,2	K562	blood:
5	chr14:31856402..31859394-chr14:31860227..31863431,5	K562	blood:
6	chr14:31887818..31891601-chr14:31923594..31927929,15	K562	blood:
7	chr14:31675649..31677388-chr14:31795020..31796590,2	MCF-7	breast:
8	chr14:31819147..31821275-chr14:31824530..31827299,2	K562	blood:
9	chr14:31813244..31815741-chr14:31818339..31820763,3	K562	blood:
10	chr14:31826783..31829136-chr14:31888128..31890076,2	MCF-7	breast:
11	chr14:31675912..31678861-chr14:31887650..31889789,3	K562	blood:
12	chr14:31889397..31890218-chr9:91933424..91934086,2	Hela-S3	cervix:
13	chr14:31854067..31858154-chr14:31887468..31890013,3	MCF-7	breast:
14	chr14:31888596..31889246-chr8:110346351..110347121,2	Hela-S3	cervix:
15	chr14:31890242..31892614-chr14:31901862..31904809,2	MCF-7	breast:
16	chr14:31861407..31863284-chr14:31887639..31889155,2	K562	blood:
17	chr14:31899509..31901563-chr14:31901913..31904667,2	K562	blood:
18	chr14:31899509..31901563-chr14:31901913..31904667,2	K562	blood:
19	chr14:31705909..31710425-chr14:31710546..31713834,4	K562	blood:
20	chr14:31900629..31902248-chr14:31924546..31926804,2	MCF-7	breast:
21	chr14:31854067..31858154-chr14:31887468..31890013,3	MCF-7	breast:
22	chr14:31868409..31871104-chr14:31872239..31873925,2	K562	blood:
23	chr14:31671940..31673668-chr14:31776880..31779409,2	MCF-7	breast:
24	chr14:31677123..31678687-chr14:31776671..31778228,2	MCF-7	breast:
25	chr14:31674533..31677415-chr14:31773657..31777062,4	MCF-7	breast:
26	chr14:31675776..31677438-chr14:31780625..31782203,2	MCF-7	breast:
27	chr14:31675532..31678117-chr14:31730710..31734144,6	MCF-7	breast:
28	chr14:31784409..31786854-chr14:31787339..31791059,3	MCF-7	breast:
29	chr14:31864866..31867235-chr14:31869226..31871358,2	MCF-7	breast:
30	chr14:31720575..31722092-chr14:31768141..31769654,2	MCF-7	breast:
31	chr14:31735111..31736764-chr14:31740143..31742182,2	MCF-7	breast:
32	chr14:31890242..31892614-chr14:31901862..31904809,2	MCF-7	breast:
33	chr14:31676274..31678860-chr14:31889133..31891124,4	MCF-7	breast:
34	chr14:31674894..31678843-chr14:31820939..31826444,5	MCF-7	breast:
35	chr14:31781406..31781906-chr19:27732227..27733066,2	MCF-7	breast:
36	chr14:31705909..31709311-chr14:31711142..31713834,3	K562	blood:
37	chr14:31675991..31678700-chr14:31818216..31819802,2	MCF-7	breast:
38	chr14:31864866..31867235-chr14:31869226..31871358,2	MCF-7	breast:
39	chr14:31720575..31722092-chr14:31768141..31769654,2	MCF-7	breast:
40	chr14:31675418..31678639-chr14:31811864..31816181,5	MCF-7	breast:
41	chr14:31888742..31889382-chr3:41241031..41241649,2	Hela-S3	cervix:
42	chr14:31732131..31735050-chr14:31739245..31741338,2	K562	blood:
43	chr14:31881996..31884911-chr14:31918681..31921369,2	MCF-7	breast:
44	chr14:31677046..31680336-chr14:31784092..31788238,4	K562	blood:
45	chr13:37574206..37574708-chr14:31889229..31890178,2	Hela-S3	cervix:
46	chr14:31676619..31677277-chr14:31889333..31889964,2	K562	blood:
47	chr14:31735111..31736764-chr14:31740143..31742182,2	MCF-7	breast:
48	chr14:31887046..31892106-chr14:31923824..31928892,9	K562	blood:
49	chr14:31677416..31678964-chr14:31720140..31723072,2	K562	blood:
50	chr14:31677046..31680336-chr14:31784092..31787188,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUBPL-1	chr14:31889492-31889791	ENSG00000250365
2	lnc-NUBPL-1	chr14:31891054-31891174	ENSG00000250365
3	lnc-NUBPL-1	chr14:31891054-31891174	ENSG00000250365
4	lnc-HEATR5A-1	chr14:31721229-31721429	NONHSAT036276
5	lnc-NUBPL-1	chr14:31891050-31891174	ENSG00000250365
6	lnc-HEATR5A-1	chr14:31732507-31733032	NONHSAT036276
7	lnc-NUBPL-1	chr14:31889964-31890183	ENSG00000250365
8	lnc-NUBPL-1	chr14:31890150-31890183	ENSG00000250365

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	HEATR5A	hsa-miR-124-3p	chr14:31761780-31761799

Variant related genes	Relation type
ENSG00000263784	TF binding region
ENSG00000250365	TF binding region
ENSG00000202402	TF binding region
ENSG00000257831	TF binding region
HEATR5A	TF binding region
ENSG00000199291	TF binding region
ENSG00000263784	CpG island
ENSG00000250365	CpG island
ENSG00000202402	CpG island
ENSG00000257831	CpG island
HEATR5A	CpG island
ENSG00000199291	CpG island
ENSG00000204388	chromatin interactions
ENSG00000092108	chromatin interactions
ENSG00000129493	chromatin interactions
ENSG00000120699	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000168036	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000199291	chromatin interactions
ENSG00000270820	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000129480	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000120697	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000120526	chromatin interactions
YTHDC1	miRNA target sites
ALG2	miRNA target sites
CCNG1	miRNA target sites
SLC26A2	miRNA target sites

Extended variants
information (count: 7488 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7488 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534997330	chr14:31711264-31711265	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs192687652	chr14:31711273-31711274	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs143902363	chr14:31711281-31711282	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs74042193	chr14:31711302-31711303	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs376826450	chr14:31711312-31711313	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs10136337	chr14:31711348-31711349	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs562202484	chr14:31711355-31711356	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs529490788	chr14:31711356-31711357	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs371169207	chr14:31711366-31711367	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs562850058	chr14:31711401-31711402	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs533410658	chr14:31711410-31711411	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs551376427	chr14:31711421-31711422	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs183391259	chr14:31711523-31711524	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs144871175	chr14:31711539-31711540	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs187733664	chr14:31711563-31711564	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs575757557	chr14:31711590-31711591	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs554824497	chr14:31711600-31711601	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs10148827	chr14:31711620-31711621	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs142100206	chr14:31711626-31711627	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs578010536	chr14:31711655-31711656	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs151176821	chr14:31711665-31711666	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs192390314	chr14:31711725-31711726	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs573196607	chr14:31711819-31711820	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs540617425	chr14:31711860-31711861	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564778277	chr14:31711906-31711907	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs571620803	chr14:31711911-31711912	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs367864390	chr14:31711944-31711945	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs573755183	chr14:31711950-31711951	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs184350690	chr14:31711972-31711973	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs532331118	chr14:31712002-31712003	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs118107586	chr14:31712016-31712017	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs115293524	chr14:31712022-31712023	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs558336551	chr14:31712046-31712047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147093233	chr14:31712071-31712072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs377509058	chr14:31712075-31712076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369561181	chr14:31712082-31712083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577677741	chr14:31712194-31712195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545414417	chr14:31712203-31712204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560832514	chr14:31712273-31712274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114028645	chr14:31712318-31712319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189722257	chr14:31712352-31712353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs567379666	chr14:31712354-31712355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs531400583	chr14:31712429-31712430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140281841	chr14:31712431-31712432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370380785	chr14:31712475-31712476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146995126	chr14:31712485-31712486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538816921	chr14:31712496-31712497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs73267405	chr14:31712498-31712499	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs565918229	chr14:31712563-31712564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533947547	chr14:31712565-31712566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:4305 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31707800-31712800	Weak transcription	Lung	lung
2	chr14:31707800-31713400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:31707800-31730800	Weak transcription	Pancreas	Pancrea
4	chr14:31709000-31713800	Enhancers	K562	blood
5	chr14:31710200-31712000	Enhancers	HepG2	liver
6	chr14:31710400-31711400	Enhancers	GM12878-XiMat	blood
7	chr14:31710400-31711400	Enhancers	Hela-S3	cervix
8	chr14:31710600-31711400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr14:31710600-31711600	Enhancers	Colon Smooth Muscle	Colon
10	chr14:31710600-31715200	Enhancers	Stomach Mucosa	stomach
11	chr14:31710800-31711400	Enhancers	Primary T cells fromperipheralblood	blood
12	chr14:31710800-31711400	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr14:31710800-31711400	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr14:31710800-31711400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
15	chr14:31710800-31711400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr14:31710800-31711400	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr14:31710800-31711400	Enhancers	A549	lung
18	chr14:31710800-31711600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr14:31710800-31711600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:31710800-31711600	Flanking Active TSS	Rectal Smooth Muscle	rectum
21	chr14:31710800-31711800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr14:31710800-31711800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr14:31710800-31711800	Enhancers	Left Ventricle	heart
24	chr14:31710800-31711800	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr14:31710800-31712000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr14:31710800-31712000	Enhancers	HMEC	breast
27	chr14:31710800-31712200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr14:31710800-31712400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr14:31711000-31711400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr14:31711000-31711400	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
31	chr14:31711000-31711400	Enhancers	Esophagus	oesophagus
32	chr14:31711000-31711400	Enhancers	HSMMtube	muscle
33	chr14:31711000-31711400	Flanking Active TSS	NHDF-Ad	bronchial
34	chr14:31711000-31711400	Flanking Active TSS	NHLF	lung
35	chr14:31711000-31711400	Flanking Active TSS	Osteobl	bone
36	chr14:31711000-31711600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr14:31711000-31711600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr14:31711000-31711600	Enhancers	Duodenum Mucosa	Duodenum
39	chr14:31711000-31711600	Enhancers	Small Intestine	intestine
40	chr14:31711000-31711800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr14:31711000-31711800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr14:31711000-31711800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr14:31711000-31711800	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr14:31711200-31711400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr14:31711200-31711400	Flanking Active TSS	Ovary	ovary
46	chr14:31711200-31711400	Flanking Active TSS	Stomach Smooth Muscle	stomach
47	chr14:31711200-31711600	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr14:31711200-31711600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr14:31711200-31711600	Enhancers	Liver	Liver
50	chr14:31711200-31711600	Weak transcription	Fetal Lung	lung

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