Variant report

Variant	nsv542046
Chromosome Location	chr14:38294270-38436127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:38303625-38303740	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:38372828-38373175	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:38318201-38318889	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:38333587-38335172	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:38359344-38359690	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:38343659-38344387	HepG2	liver:	n/a	n/a
7	ATF2	chr14:38343770-38344211	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr14:38343844-38344202	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr14:38343911-38344112	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:38408874-38409167	HepG2	liver:	n/a	n/a
11	BHLHE40	chr14:38334090-38334887	HepG2	liver:	n/a	n/a
12	BHLHE40	chr14:38343887-38344195	K562	blood:	n/a	n/a
13	BRCA1	chr14:38343797-38344206	HepG2	liver:	n/a	n/a
14	BRCA1	chr14:38334052-38334677	HepG2	liver:	n/a	n/a
15	CBX3	chr14:38343833-38344356	HCT-116	colon:	n/a	n/a
16	CEBPB	chr14:38313369-38313818	MCF-7	breast:	n/a	chr14:38313601-38313612
17	CEBPB	chr14:38324864-38325132	K562	blood:	n/a	chr14:38324999-38325012 chr14:38325000-38325011 chr14:38324999-38325010 chr14:38324999-38325012 chr14:38324999-38325012
18	CEBPB	chr14:38334047-38334670	HepG2	liver:	n/a	n/a
19	CEBPB	chr14:38344966-38345064	K562	blood:	n/a	chr14:38345020-38345033 chr14:38345020-38345033 chr14:38345022-38345033 chr14:38345020-38345031
20	CEBPB	chr14:38385588-38385892	HepG2	liver:	n/a	chr14:38385721-38385732
21	CEBPB	chr14:38313389-38313845	A549	lung:	n/a	chr14:38313601-38313612
22	CEBPB	chr14:38407461-38407801	HepG2	liver:	n/a	chr14:38407624-38407635 chr14:38407622-38407633 chr14:38407641-38407654
23	CEBPB	chr14:38313446-38313776	A549	lung:	n/a	chr14:38313601-38313612
24	CEBPB	chr14:38334795-38335133	A549	lung:	n/a	chr14:38334963-38334974 chr14:38334963-38334972 chr14:38334963-38334972 chr14:38334961-38334974 chr14:38334963-38334972 chr14:38334961-38334974 chr14:38334963-38334972
25	CEBPB	chr14:38369817-38370145	IMR90	lung:	n/a	chr14:38369997-38370008
26	CEBPB	chr14:38385527-38385864	MCF-7	breast:	n/a	chr14:38385721-38385732
27	CEBPB	chr14:38313359-38313792	HepG2	liver:	n/a	chr14:38313601-38313612
28	CEBPB	chr14:38365037-38365329	HepG2	liver:	n/a	chr14:38365146-38365163 chr14:38365149-38365160
29	CEBPB	chr14:38340338-38340579	A549	lung:	n/a	chr14:38340453-38340464
30	CEBPB	chr14:38313423-38313757	IMR90	lung:	n/a	chr14:38313601-38313612
31	CEBPB	chr14:38385568-38385866	IMR90	lung:	n/a	chr14:38385721-38385732
32	CEBPB	chr14:38369819-38370154	HepG2	liver:	n/a	chr14:38369997-38370008
33	CEBPB	chr14:38365572-38365735	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:38340277-38340638	HepG2	liver:	n/a	chr14:38340453-38340464
35	CEBPB	chr14:38313496-38313703	H1-hESC	embryonic stem cell:	n/a	chr14:38313601-38313612
36	CEBPB	chr14:38324828-38325176	IMR90	lung:	n/a	chr14:38324999-38325012 chr14:38325000-38325011 chr14:38324999-38325010 chr14:38324999-38325012 chr14:38324999-38325012
37	CEBPB	chr14:38334834-38335047	H1-hESC	embryonic stem cell:	n/a	chr14:38334963-38334974 chr14:38334963-38334972 chr14:38334963-38334972 chr14:38334961-38334974 chr14:38334963-38334972 chr14:38334961-38334974 chr14:38334963-38334972
38	CEBPB	chr14:38407480-38407800	IMR90	lung:	n/a	chr14:38407624-38407635 chr14:38407622-38407633 chr14:38407641-38407654
39	CEBPB	chr14:38343603-38344165	HepG2	liver:	n/a	n/a
40	CEBPB	chr14:38324916-38325097	A549	lung:	n/a	chr14:38324999-38325012 chr14:38325000-38325011 chr14:38324999-38325010 chr14:38324999-38325012 chr14:38324999-38325012
41	CEBPB	chr14:38344864-38345275	HepG2	liver:	n/a	chr14:38345020-38345033 chr14:38345020-38345033 chr14:38345022-38345033 chr14:38345020-38345031
42	CEBPB	chr14:38376350-38376516	HepG2	liver:	n/a	chr14:38376407-38376418
43	CEBPB	chr14:38358287-38358753	ECC-1	luminal epithelium:	n/a	n/a
44	CEBPB	chr14:38327984-38328292	HepG2	liver:	n/a	chr14:38327987-38328000
45	CEBPB	chr14:38334777-38335104	IMR90	lung:	n/a	chr14:38334963-38334974 chr14:38334963-38334972 chr14:38334963-38334972 chr14:38334961-38334974 chr14:38334963-38334972 chr14:38334961-38334974 chr14:38334963-38334972
46	CEBPB	chr14:38313457-38313687	ECC-1	luminal epithelium:	n/a	chr14:38313601-38313612
47	CEBPB	chr14:38318261-38318533	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:38344902-38345155	IMR90	lung:	n/a	chr14:38345020-38345033 chr14:38345020-38345033 chr14:38345022-38345033 chr14:38345020-38345031
49	CEBPB	chr14:38313415-38313793	HepG2	liver:	n/a	chr14:38313601-38313612
50	CEBPB	chr14:38320301-38320598	HepG2	liver:	n/a	chr14:38320452-38320463 chr14:38320451-38320462

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:38400115-38400165	GM12892	blood:	n/a
2	chr14:38371657-38371707	HRPEpiC	eye:	n/a
3	chr14:38363538-38363588	ProgFib	skin:	n/a
4	chr14:38363538-38363588	LNCaP	prostate:	n/a
5	chr14:38371922-38371972	HNPCEpiC	eye:	n/a
6	chr14:38371922-38371972	SAEC	small airway:	n/a
7	chr14:38371657-38371707	HRE	kidney:	n/a
8	chr14:38363538-38363588	SK-N-SH_RA	brain:	n/a
9	chr14:38340164-38340214	PANC-1	pancreas:	n/a
10	chr14:38371657-38371707	SK-N-MC	brain:	n/a
11	chr14:38400115-38400165	MCF-7	breast:	n/a
12	chr14:38400115-38400165	U87	brain:	n/a
13	chr14:38401512-38401562	PFSK-1	brain:	n/a
14	chr14:38371922-38371972	NB4	blood:	n/a
15	chr14:38363538-38363588	AoSMC	blood vessel:	n/a
16	chr14:38363538-38363588	HCPEpiC	choroid plexus:	n/a
17	chr14:38371657-38371707	HNPCEpiC	eye:	n/a
18	chr14:38401512-38401562	HCF	heart:	n/a
19	chr14:38363538-38363588	A549	lung:	n/a
20	chr14:38400115-38400165	AG04449	skin:	fetal
21	chr14:38363538-38363588	HCT-116	colon:	n/a
22	chr14:38340164-38340214	PrEC	prostate:	n/a
23	chr14:38340164-38340214	AG04450	lung:	fetal
24	chr14:38371657-38371707	NH-A	brain:	n/a
25	chr14:38363538-38363588	GM19239	blood:	n/a
26	chr14:38340164-38340214	HIPEpiC	eye:	n/a
27	chr14:38400115-38400165	BJ	skin:	n/a
28	chr14:38401512-38401562	SAEC	small airway:	n/a
29	chr14:38340164-38340214	Jurkat	blood:	n/a
30	chr14:38401512-38401562	H1-hESC	embryonic stem cell:	embryo
31	chr14:38371922-38371972	MCF-7	breast:	n/a
32	chr14:38371657-38371707	Jurkat	blood:	n/a
33	chr14:38401512-38401562	A549	lung:	n/a
34	chr14:38371922-38371972	AG04450	lung:	fetal
35	chr14:38400115-38400165	HEEpiC	esophagus:	n/a
36	chr14:38401512-38401562	CMK	blood:	n/a
37	chr14:38371922-38371972	BE2_C	brain:	n/a
38	chr14:38363538-38363588	GM06990	blood:	n/a
39	chr14:38400115-38400165	HRCEpiC	kidney:	n/a
40	chr14:38400115-38400165	ProgFib	skin:	n/a
41	chr14:38371657-38371707	A549	lung:	n/a
42	chr14:38401512-38401562	HMEC	breast:	n/a
43	chr14:38340164-38340214	MCF-7	breast:	n/a
44	chr14:38401512-38401562	Jurkat	blood:	n/a
45	chr14:38400115-38400165	HCF	heart:	n/a
46	chr14:38363538-38363588	HRPEpiC	eye:	n/a
47	chr14:38371922-38371972	HRPEpiC	eye:	n/a
48	chr14:38371657-38371707	MCF10A-Er-Src	breast:	n/a
49	chr14:38371922-38371972	SK-N-MC	brain:	n/a
50	chr14:38363538-38363588	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:38177834..38178487-chr14:38343555..38344210,2	MCF-7	breast:
2	chr14:38062426..38066513-chr14:38338443..38346839,18	MCF-7	breast:
3	chr14:38051959..38054896-chr14:38346073..38349054,2	MCF-7	breast:
4	chr14:38372602..38374691-chr14:38377284..38379028,2	MCF-7	breast:
5	chr14:38178183..38179217-chr14:38343472..38344512,5	MCF-7	breast:
6	chr14:38339276..38342707-chr14:38343768..38347145,3	MCF-7	breast:
7	chr14:38397859..38399776-chr14:38406213..38408130,2	MCF-7	breast:
8	chr14:38397859..38399776-chr14:38406213..38408130,2	MCF-7	breast:
9	chr14:38338833..38341519-chr14:38342499..38345279,2	MCF-7	breast:
10	chr14:38363021..38365119-chr14:38365586..38368317,2	MCF-7	breast:
11	chr14:38339276..38342707-chr14:38343768..38347145,3	MCF-7	breast:
12	chr14:38343955..38346094-chr14:38346760..38348457,2	MCF-7	breast:
13	chr14:38363021..38365119-chr14:38365586..38368317,2	MCF-7	breast:
14	chr14:38338833..38341519-chr14:38342499..38345279,2	MCF-7	breast:
15	chr14:37724664..37726988-chr14:38331777..38333562,2	MCF-7	breast:
16	chr14:38060189..38065879-chr14:38339920..38349339,20	MCF-7	breast:
17	chr14:38343955..38346094-chr14:38346760..38348457,2	MCF-7	breast:
18	chr14:38056746..38059083-chr14:38363861..38366801,2	MCF-7	breast:
19	chr14:38357219..38359040-chr6:27806229..27807862,2	MCF-7	breast:
20	chr14:38060569..38062165-chr14:38339643..38341361,2	MCF-7	breast:
21	chr14:38063353..38065330-chr14:38297774..38300460,2	MCF-7	breast:
22	chr14:38372874..38373419-chr14:39069490..39070036,2	MCF-7	breast:
23	chr14:37720959..37721697-chr14:38343187..38344314,3	MCF-7	breast:
24	chr14:38372602..38374691-chr14:38377284..38379028,2	MCF-7	breast:
25	chr14:38317873..38320611-chr14:38331977..38333787,2	MCF-7	breast:
26	chr14:38372517..38373229-chr14:38666364..38667063,2	MCF-7	breast:
27	chr14:38372603..38373391-chr14:38619012..38619723,2	MCF-7	breast:
28	chr14:38288642..38290464-chr14:38293057..38295277,2	MCF-7	breast:
29	chr14:38179396..38181240-chr14:38325278..38326866,2	MCF-7	breast:
30	chr14:38365851..38368436-chr14:38371004..38373198,2	MCF-7	breast:
31	chr14:38317873..38320611-chr14:38331977..38333787,2	MCF-7	breast:
32	chr14:38055655..38059490-chr14:38342768..38346428,4	MCF-7	breast:
33	chr14:38178580..38179381-chr14:38343573..38344582,8	MCF-7	breast:
34	chr14:38063198..38065699-chr14:38312720..38314688,2	MCF-7	breast:
35	chr14:38372704..38373564-chr14:39336508..39337178,3	K562	blood:
36	chr14:38178359..38181904-chr14:38339541..38344216,4	MCF-7	breast:
37	chr14:37715448..37716190-chr14:38343588..38344540,3	MCF-7	breast:
38	chr14:38054286..38055806-chr14:38336745..38339551,2	MCF-7	breast:
39	chr14:37715320..37716132-chr14:38343587..38344326,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MIPOL1-6	chr14:38332971-38338005	NONHSAT036473
2	lnc-CLEC14A-4	chr14:38376599-38376755	l_970_chr14:38376598-38429748_brain
3	lnc-CLEC14A-4	chr14:38376771-38378159	l_970_chr14:38376598-38429748_brain
4	lnc-SSTR1-3	chr14:38397062-38397296	NONHSAT036476
5	lnc-SSTR1-3	chr14:38385712-38385759	NONHSAT036476
6	lnc-SSTR1-3	chr14:38385713-38385759	XLOC_010808
7	lnc-FOXA1-2	chr14:38371221-38371577	ENSG00000259091.1
8	lnc-SSTR1-3	chr14:38392665-38395930	NONHSAT036476
9	lnc-MIPOL1-6	chr14:38350870-38351237	NONHSAT036473
10	lnc-SSTR1-4	chr14:38405430-38405683	NONHSAT036478
11	lnc-SSTR1-4	chr14:38405430-38405683	FPKM1_group_8712_transcript_1
12	lnc-SSTR1-3	chr14:38397063-38397296	XLOC_010808
13	lnc-SSTR1-4	chr14:38408615-38408764	NONHSAT036478
14	lnc-FOXA1-2	chr14:38371221-38371329	XLOC_010999
15	lnc-FOXA1-2	chr14:38365265-38368615	XLOC_010999
16	lnc-FOXA1-2	chr14:38370081-38370497	ENSG00000259091.1
17	lnc-SSTR1-4	chr14:38408615-38408629	FPKM1_group_8712_transcript_1
18	lnc-SSTR1-3	chr14:38395384-38395502	XLOC_010808
19	lnc-MIPOL1-6	chr14:38343586-38344006	NONHSAT036473
20	lnc-CLEC14A-4	chr14:38429696-38429748	l_970_chr14:38376598-38429748_brain
21	lnc-MIPOL1-6	chr14:38320042-38321184	NONHSAT036473

Variant related genes	Relation type
RNU6-1277P	TF binding region
LINC00517	TF binding region
TTC6	TF binding region
RNU6-1277P	CpG island
LINC00517	CpG island
TTC6	CpG island
ENSG00000259091	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000233822	chromatin interactions

Extended variants
information (count: 2963 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2963 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77720149	chr14:38294331-38294332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576383980	chr14:38294332-38294333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370241636	chr14:38294339-38294340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188560608	chr14:38294341-38294342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565356598	chr14:38294355-38294356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527899184	chr14:38294407-38294408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368066820	chr14:38294524-38294525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs374951860	chr14:38294554-38294555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534253757	chr14:38294579-38294580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561256059	chr14:38294586-38294587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530281612	chr14:38294590-38294591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117922002	chr14:38294645-38294646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557821854	chr14:38294669-38294670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs569591369	chr14:38294700-38294701	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs202124305	chr14:38294767-38294768	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs117285172	chr14:38294806-38294807	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs192864487	chr14:38294878-38294879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185434213	chr14:38294900-38294901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371299942	chr14:38294903-38294904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147437317	chr14:38294930-38294931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540080475	chr14:38294944-38294945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568367586	chr14:38294972-38294973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537391750	chr14:38294985-38294986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6571823	chr14:38295029-38295030	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs576384664	chr14:38295112-38295113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189293423	chr14:38295115-38295116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139177357	chr14:38295161-38295162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566864751	chr14:38295172-38295173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541229549	chr14:38295187-38295188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7154349	chr14:38295231-38295232	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs574682639	chr14:38295242-38295243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554295259	chr14:38295257-38295258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563987348	chr14:38295277-38295278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372584838	chr14:38295305-38295306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552117206	chr14:38295306-38295307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115562583	chr14:38295346-38295347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528147975	chr14:38295359-38295360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201873484	chr14:38295366-38295367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372035944	chr14:38295367-38295368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555569720	chr14:38295385-38295386	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373064661	chr14:38295386-38295387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192695225	chr14:38295387-38295388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376624396	chr14:38295407-38295408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373745034	chr14:38295418-38295419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568304596	chr14:38295490-38295491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141809061	chr14:38295498-38295499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369424662	chr14:38295524-38295525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201218514	chr14:38295529-38295530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202101753	chr14:38295561-38295562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372637534	chr14:38295577-38295578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Prostate cancer	21147910	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38280400-38295600	Weak transcription	Liver	Liver
2	chr14:38293400-38294800	Enhancers	Fetal Stomach	stomach
3	chr14:38293800-38295200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:38294000-38294400	Enhancers	Stomach Smooth Muscle	stomach
5	chr14:38294000-38294400	Enhancers	HSMMtube	muscle
6	chr14:38294000-38294600	Enhancers	Fetal Lung	lung
7	chr14:38294000-38294600	Enhancers	Rectal Smooth Muscle	rectum
8	chr14:38294000-38294800	Enhancers	HepG2	liver
9	chr14:38294000-38297000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr14:38294200-38294600	Enhancers	Colon Smooth Muscle	Colon
11	chr14:38294200-38294600	Enhancers	Fetal Brain Male	brain
12	chr14:38294200-38294600	Enhancers	NH-A	brain
13	chr14:38294400-38295000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:38294600-38300400	Weak transcription	Colon Smooth Muscle	Colon
15	chr14:38295600-38296000	Enhancers	Liver	Liver
16	chr14:38304200-38304400	Enhancers	Pancreas	Pancrea
17	chr14:38304600-38308000	Weak transcription	Liver	Liver
18	chr14:38313200-38313800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr14:38313400-38315000	Enhancers	HepG2	liver
20	chr14:38315000-38317400	Weak transcription	HepG2	liver
21	chr14:38317400-38319600	Enhancers	HepG2	liver
22	chr14:38324600-38326600	Enhancers	Fetal Lung	lung
23	chr14:38324800-38325400	Enhancers	Liver	Liver
24	chr14:38325400-38333200	Weak transcription	Liver	Liver
25	chr14:38327000-38329200	Enhancers	HepG2	liver
26	chr14:38329200-38331400	Weak transcription	HepG2	liver
27	chr14:38331400-38331600	Enhancers	Esophagus	oesophagus
28	chr14:38331400-38332000	Enhancers	HepG2	liver
29	chr14:38331600-38333400	Weak transcription	Esophagus	oesophagus
30	chr14:38331800-38332000	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr14:38332000-38333000	Weak transcription	HepG2	liver
32	chr14:38332400-38343600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr14:38333000-38333400	Enhancers	HepG2	liver
34	chr14:38333200-38334600	Enhancers	Liver	Liver
35	chr14:38333400-38334800	Enhancers	Esophagus	oesophagus
36	chr14:38333400-38334800	Enhancers	Stomach Mucosa	stomach
37	chr14:38333400-38335000	Enhancers	Stomach Smooth Muscle	stomach
38	chr14:38333400-38335600	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr14:38333400-38335600	Enhancers	Colon Smooth Muscle	Colon
40	chr14:38333400-38335600	Enhancers	Rectal Smooth Muscle	rectum
41	chr14:38333400-38335800	Flanking Active TSS	HepG2	liver
42	chr14:38333600-38334000	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr14:38333600-38334200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr14:38334000-38334200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr14:38334000-38334400	Enhancers	Brain Cingulate Gyrus	brain
46	chr14:38334000-38334400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr14:38334000-38334600	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr14:38334000-38334800	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr14:38334000-38334800	Enhancers	A549	lung
50	chr14:38334000-38334800	Enhancers	NHDF-Ad	bronchial

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