Variant report

Variant	esv12377
Chromosome Location	chr3:49720751-49735851
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1071)
CpG islands
(count:1222)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1071 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:49726762-49727051	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:49726435-49726638	K562	blood:	n/a	n/a
3	ATF1	chr3:49726441-49726642	K562	blood:	n/a	n/a
4	ATF2	chr3:49726715-49727287	GM12878	blood:	n/a	n/a
5	ATF2	chr3:49726771-49727184	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr3:49726826-49727192	GM12878	blood:	n/a	n/a
7	ATF3	chr3:49726743-49727206	A549	lung:	n/a	n/a
8	ATF3	chr3:49726774-49727187	A549	lung:	n/a	n/a
9	BATF	chr3:49726459-49727151	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:49726800-49727197	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:49722968-49723129	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:49726963-49727227	GM12878	blood:	n/a	chr3:49727192-49727205
13	BCL3	chr3:49726720-49727192	A549	lung:	n/a	n/a
14	BCL3	chr3:49726646-49727262	A549	lung:	n/a	chr3:49727192-49727205
15	BCLAF1	chr3:49726739-49727289	GM12878	blood:	n/a	chr3:49727192-49727205
16	BCLAF1	chr3:49726861-49727288	K562	blood:	n/a	chr3:49727192-49727205
17	BCLAF1	chr3:49726698-49727308	GM12878	blood:	n/a	chr3:49727192-49727205
18	BHLHE40	chr3:49726433-49727116	K562	blood:	n/a	n/a
19	BHLHE40	chr3:49726769-49727171	HepG2	liver:	n/a	n/a
20	BHLHE40	chr3:49726769-49727129	GM12878	blood:	n/a	n/a
21	BRCA1	chr3:49726858-49727121	HepG2	liver:	n/a	n/a
22	BRCA1	chr3:49726122-49726173	HepG2	liver:	n/a	n/a
23	CBX3	chr3:49723474-49724174	K562	blood:	n/a	n/a
24	CBX3	chr3:49725844-49727257	K562	blood:	n/a	n/a
25	CBX3	chr3:49727290-49728239	K562	blood:	n/a	n/a
26	CBX3	chr3:49726336-49727034	K562	blood:	n/a	n/a
27	CCNT2	chr3:49726862-49727206	K562	blood:	n/a	n/a
28	CEBPB	chr3:49725999-49726205	K562	blood:	n/a	chr3:49726131-49726142
29	CEBPB	chr3:49726820-49727185	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr3:49725976-49726336	HepG2	liver:	n/a	chr3:49726131-49726142
31	CEBPB	chr3:49726094-49726245	HepG2	liver:	n/a	chr3:49726131-49726142
32	CEBPB	chr3:49725936-49727036	K562	blood:	n/a	chr3:49726131-49726142
33	CEBPB	chr3:49725976-49726402	HepG2	liver:	n/a	chr3:49726131-49726142
34	CEBPB	chr3:49726073-49726639	K562	blood:	n/a	chr3:49726131-49726142
35	CEBPB	chr3:49727017-49727128	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:49726932-49727132	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:49726303-49727240	GM12878	blood:	n/a	n/a
38	CEBPD	chr3:49726779-49727094	HepG2	liver:	n/a	n/a
39	CEBPD	chr3:49726080-49726365	HepG2	liver:	n/a	chr3:49726130-49726141
40	CEBPD	chr3:49727848-49728263	K562	blood:	n/a	n/a
41	CEBPD	chr3:49726053-49727801	K562	blood:	n/a	chr3:49726130-49726141
42	CEBPD	chr3:49726024-49726402	HepG2	liver:	n/a	chr3:49726130-49726141
43	CHD1	chr3:49726958-49727160	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr3:49727259-49727450	GM12878	blood:	n/a	n/a
45	CHD1	chr3:49726620-49726904	GM12878	blood:	n/a	n/a
46	CHD2	chr3:49726601-49727189	K562	blood:	n/a	n/a
47	CHD2	chr3:49726690-49727463	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr3:49726841-49727189	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr3:49726138-49726277	HepG2	liver:	n/a	n/a
50	CHD2	chr3:49726742-49727165	HepG2	liver:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:49727474-49727524	HCM	heart:	n/a
2	chr3:49723947-49723997	HepG2	liver:	n/a
3	chr3:49727474-49727524	HCM	heart:	n/a
4	chr3:49723947-49723997	HepG2	liver:	n/a
5	chr3:49727474-49727524	T-47D	breast:	n/a
6	chr3:49726922-49726972	ECC-1	luminal epithelium:	n/a
7	chr3:49722237-49722287	HRE	kidney:	n/a
8	chr3:49720819-49720869	HCF	heart:	n/a
9	chr3:49727025-49727075	HUVEC	blood vessel:	n/a
10	chr3:49727025-49727075	Jurkat	blood:	n/a
11	chr3:49724254-49724304	K562	blood:	n/a
12	chr3:49724254-49724304	Caco-2	colon:	n/a
13	chr3:49722237-49722287	SK-N-SH	brain:	n/a
14	chr3:49726910-49726960	GM06990	blood:	n/a
15	chr3:49723245-49723295	ovcar-3	ovarian:	n/a
16	chr3:49726775-49726825	CMK	blood:	n/a
17	chr3:49726928-49726978	GM06990	blood:	n/a
18	chr3:49726922-49726972	NB4	blood:	n/a
19	chr3:49722237-49722287	PANC-1	pancreas:	n/a
20	chr3:49726922-49726972	T-47D	breast:	n/a
21	chr3:49726922-49726972	GM19239	blood:	n/a
22	chr3:49724291-49724341	AoSMC	blood vessel:	n/a
23	chr3:49726775-49726825	NH-A	brain:	n/a
24	chr3:49723947-49723997	A549	lung:	n/a
25	chr3:49723947-49723997	GM19239	blood:	n/a
26	chr3:49726785-49726835	ovcar-3	ovarian:	n/a
27	chr3:49726443-49726493	NT2-D1	testis:	n/a
28	chr3:49727222-49727272	NB4	blood:	n/a
29	chr3:49726443-49726493	Hepatocyte	liver:	n/a
30	chr3:49727474-49727524	HEK293	kidney:	embryo
31	chr3:49726785-49726835	AG04450	lung:	fetal
32	chr3:49727025-49727075	SK-N-SH	brain:	n/a
33	chr3:49726910-49726960	LNCaP	prostate:	n/a
34	chr3:49726443-49726493	HIPEpiC	eye:	n/a
35	chr3:49727222-49727272	HRPEpiC	eye:	n/a
36	chr3:49723245-49723295	AG04450	lung:	fetal
37	chr3:49726912-49726962	NH-A	brain:	n/a
38	chr3:49727322-49727372	AG10803	skin:	n/a
39	chr3:49726785-49726835	HEK293	kidney:	embryo
40	chr3:49726775-49726825	ProgFib	skin:	n/a
41	chr3:49724254-49724304	BJ	skin:	n/a
42	chr3:49722237-49722287	BJ	skin:	n/a
43	chr3:49726443-49726493	AG04450	lung:	fetal
44	chr3:49720819-49720869	NHDF-neo	bronchial:	n/a
45	chr3:49726922-49726972	HEK293	kidney:	embryo
46	chr3:49727025-49727075	SAEC	small airway:	n/a
47	chr3:49724291-49724341	HRCEpiC	kidney:	n/a
48	chr3:49727025-49727075	PFSK-1	brain:	n/a
49	chr3:49726151-49726201	LNCaP	prostate:	n/a
50	chr3:49726443-49726493	NHDF-neo	bronchial:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49727338..49730126-chr3:49733777..49735933,2	K562	blood:
2	chr3:49724349..49727675-chr3:49755739..49757510,3	MCF-7	breast:
3	chr3:49725473..49727934-chr3:49733228..49735163,2	MCF-7	breast:
4	chr3:49715255..49718446-chr3:49718549..49721372,3	MCF-7	breast:
5	chr3:49719547..49721441-chr3:49726309..49728909,2	K562	blood:
6	chr3:49711727..49717769-chr3:49722772..49726950,7	K562	blood:
7	chr3:49720877..49722933-chr3:49723247..49725096,3	K562	blood:
8	chr3:49708866..49715375-chr3:49724746..49730407,6	K562	blood:
9	chr1:17086818..17089262-chr3:49723617..49726310,2	MCF-7	breast:
10	chr3:49719726..49722448-chr3:49723596..49725872,2	K562	blood:
11	chr1:16968825..16972400-chr3:49724902..49730445,9	MCF-7	breast:
12	chr3:49719726..49722448-chr3:49723596..49725872,2	K562	blood:
13	chr3:49724739..49727802-chr3:49735823..49739048,3	MCF-7	breast:
14	chr1:16970617..16971914-chr3:49726307..49727625,5	Hela-S3	cervix:
15	chr3:49735446..49741255-chr3:49749875..49755830,7	K562	blood:
16	chr1:16969769..16972744-chr3:49724987..49728952,10	MCF-7	breast:
17	chr3:49734358..49736524-chr3:49759903..49761802,2	K562	blood:
18	chr3:49719547..49721441-chr3:49726309..49728909,2	K562	blood:
19	chr3:49709764..49714141-chr3:49724462..49728582,8	MCF-7	breast:
20	chr1:16840059..16842019-chr3:49726620..49728606,2	MCF-7	breast:
21	chr3:49448668..49451033-chr3:49723995..49726731,2	MCF-7	breast:
22	chr3:49722536..49724153-chr3:49724898..49727146,2	MCF-7	breast:
23	chr1:16970672..16971760-chr3:49726371..49727463,9	MCF-7	breast:
24	chr3:49727338..49730126-chr3:49733777..49735933,2	K562	blood:
25	chr1:16965534..16967536-chr3:49731368..49733406,2	MCF-7	breast:
26	chr3:49720877..49722933-chr3:49723247..49725096,3	K562	blood:
27	chr3:49715099..49716706-chr3:49727000..49728524,2	K562	blood:
28	chr3:49727014..49727624-chr9:137217199..137217737,2	HCT-116	colon:
29	chr1:16967505..16970339-chr3:49729112..49731366,2	MCF-7	breast:
30	chr1:16970425..16971927-chr3:49726367..49727791,15	HCT-116	colon:
31	chr3:49724739..49727802-chr3:49735823..49739048,3	MCF-7	breast:
32	chr1:16964923..16974624-chr3:49722461..49732046,16	K562	blood:
33	chr12:54674340..54674894-chr3:49726726..49727505,2	Hela-S3	cervix:
34	chr3:49735420..49737608-chr3:49739915..49742749,3	K562	blood:
35	chr3:49715211..49719699-chr3:49722366..49724649,4	K562	blood:
36	chr3:49724901..49726999-chr3:49761086..49763587,3	MCF-7	breast:
37	chr1:16970648..16971367-chr3:49726608..49727129,5	MCF-7	breast:
38	chr1:16968902..16969901-chr3:49728593..49729113,2	MCF-7	breast:
39	chr3:49722536..49724153-chr3:49724898..49727146,2	MCF-7	breast:
40	chr3:49710552..49715225-chr3:49718907..49727364,14	MCF-7	breast:
41	chr1:16969549..16972758-chr3:49725610..49728945,8	K562	blood:

No data

Variant related genes	Relation type
RNF123	TF binding region
ENSG00000259970	TF binding region
MST1	TF binding region
RNF123	CpG island
ENSG00000259970	CpG island
MST1	CpG island
ENSG00000164068	chromatin interactions
ENSG00000259970	chromatin interactions
ENSG00000135486	chromatin interactions
ENSG00000186301	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000176020	chromatin interactions
ENSG00000261135	chromatin interactions
ENSG00000173531	chromatin interactions
ENSG00000186715	chromatin interactions
ENSG00000215908	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000173540	chromatin interactions
ENSG00000164062	chromatin interactions

Extended variants
information (count: 761 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537120703	chr3:49720805-49720806	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs371397519	chr3:49720815-49720816	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs533443649	chr3:49720819-49720820	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs545130376	chr3:49720837-49720838	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs560104872	chr3:49720858-49720859	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs3172215	chr3:49720864-49720865	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs73834009	chr3:49720887-49720888	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs2933248	chr3:49720888-49720889	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs548966759	chr3:49720900-49720901	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs72936033	chr3:49720959-49720960	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs531925712	chr3:49720992-49720993	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs550329237	chr3:49721040-49721041	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs374185516	chr3:49721071-49721072	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs376307215	chr3:49721118-49721119	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs571785418	chr3:49721131-49721132	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs538729852	chr3:49721182-49721183	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs34404391	chr3:49721305-49721306	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs555458796	chr3:49721315-49721316	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs573659358	chr3:49721316-49721317	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs142553311	chr3:49721321-49721322	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs35870664	chr3:49721325-49721326	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs536215574	chr3:49721335-49721336	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs145946970	chr3:49721432-49721433	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs1057363	chr3:49721448-49721449	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368191700	chr3:49721510-49721511	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs369736713	chr3:49721512-49721513	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs3197999	chr3:49721532-49721533	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
28	rs201332029	chr3:49721533-49721534	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs397713690	chr3:49721542-49721543	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs397839869	chr3:49721550-49721551	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs370472291	chr3:49721554-49721555	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs1057319	chr3:49721561-49721562	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs397831743	chr3:49721571-49721572	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs373984021	chr3:49721572-49721573	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536973531	chr3:49721588-49721589	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs141594671	chr3:49721592-49721593	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs138238101	chr3:49721606-49721607	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143118019	chr3:49721607-49721608	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs141810913	chr3:49721611-49721612	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs137880382	chr3:49721614-49721615	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs200268600	chr3:49721622-49721623	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs371334584	chr3:49721623-49721624	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs577003673	chr3:49721652-49721653	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs201428113	chr3:49721653-49721654	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs545095311	chr3:49721663-49721664	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs375990239	chr3:49721717-49721718	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs150531640	chr3:49721755-49721756	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572214141	chr3:49721766-49721767	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs542575850	chr3:49721767-49721768	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs193164866	chr3:49721773-49721774	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1441 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49712200-49723800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:49712800-49722200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr3:49712800-49722200	Strong transcription	Fetal Stomach	stomach
4	chr3:49712800-49723600	Weak transcription	Right Atrium	heart
5	chr3:49712800-49726200	Weak transcription	Small Intestine	intestine
6	chr3:49713000-49721200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:49713000-49721400	Strong transcription	NHEK	skin
8	chr3:49713000-49721600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
9	chr3:49713000-49721600	Strong transcription	Brain Substantia Nigra	brain
10	chr3:49713000-49721600	Strong transcription	NHLF	lung
11	chr3:49713000-49722000	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr3:49713000-49722000	Strong transcription	Stomach Smooth Muscle	stomach
13	chr3:49713000-49722200	Strong transcription	Duodenum Smooth Muscle	Duodenum
14	chr3:49713000-49722400	Strong transcription	H9 Cell Line	embryonic stem cell
15	chr3:49713000-49722400	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr3:49713000-49722600	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr3:49713000-49722800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:49713000-49722800	Strong transcription	Thymus	Thymus
19	chr3:49713000-49723200	Weak transcription	Stomach Mucosa	stomach
20	chr3:49713000-49723400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr3:49713000-49723800	Weak transcription	Fetal Heart	heart
22	chr3:49713200-49721400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:49713200-49721400	Strong transcription	Colon Smooth Muscle	Colon
24	chr3:49713200-49721400	Strong transcription	Left Ventricle	heart
25	chr3:49713200-49721600	Strong transcription	Rectal Smooth Muscle	rectum
26	chr3:49713200-49721800	Strong transcription	H1 Cell Line	embryonic stem cell
27	chr3:49713200-49721800	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr3:49713200-49722000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr3:49713200-49722000	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr3:49713200-49722000	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr3:49713200-49722200	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr3:49713200-49722200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
33	chr3:49713200-49722200	Strong transcription	Placenta	Placenta
34	chr3:49713200-49722400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:49713200-49722400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:49713200-49722400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr3:49713200-49722400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:49713200-49722400	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr3:49713200-49722600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr3:49713200-49722600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:49713200-49722600	Strong transcription	Brain Germinal Matrix	brain
42	chr3:49713200-49722800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr3:49713200-49723000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:49713200-49723000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr3:49713400-49721400	Strong transcription	Aorta	Aorta
46	chr3:49713400-49721400	Strong transcription	Hela-S3	cervix
47	chr3:49713400-49721600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:49713400-49721600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr3:49713400-49721600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr3:49713400-49721600	Strong transcription	Fetal Lung	lung

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