Variant report

Variant	nsv560452
Chromosome Location	chr12:121341581-121357934
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	chr12:121342186-121342413	HepG2	liver:	n/a	n/a
2	ATF2	chr12:121347442-121347981	GM12878	blood:	n/a	n/a
3	ATF3	chr12:121342042-121342530	GM12878	blood:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
4	ATF3	chr12:121341947-121342470	H1-hESC	embryonic stem cell:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
5	ATF3	chr12:121342074-121342431	H1-hESC	embryonic stem cell:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
6	ATF3	chr12:121342059-121342424	K562	blood:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
7	ATF3	chr12:121342086-121342301	GM12878	blood:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
8	ATF3	chr12:121342008-121342405	K562	blood:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
9	ATF3	chr12:121342014-121342413	HepG2	liver:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
10	ATF3	chr12:121342060-121342496	HepG2	liver:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
11	ATF3	chr12:121342012-121342661	A549	lung:	n/a	chr12:121342169-121342178 chr12:121342189-121342209 chr12:121342219-121342239 chr12:121342219-121342228
12	BACH1	chr12:121342594-121342773	K562	blood:	n/a	n/a
13	BATF	chr12:121354650-121354957	GM12878	blood:	n/a	n/a
14	BATF	chr12:121347506-121347788	GM12878	blood:	n/a	n/a
15	BATF	chr12:121347483-121347901	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:121342059-121342389	A549	lung:	n/a	chr12:121342198-121342211 chr12:121342200-121342209 chr12:121342217-121342230 chr12:121342200-121342209 chr12:121342218-121342227 chr12:121342199-121342208 chr12:121342326-121342342 chr12:121342201-121342210 chr12:121342194-121342215 chr12:121342213-121342234
17	BHLHE40	chr12:121342008-121342596	GM12878	blood:	n/a	chr12:121342198-121342211 chr12:121342200-121342209 chr12:121342217-121342230 chr12:121342200-121342209 chr12:121342218-121342227 chr12:121342199-121342208 chr12:121342326-121342342 chr12:121342201-121342210 chr12:121342194-121342215 chr12:121342213-121342234
18	BHLHE40	chr12:121341800-121342724	HepG2	liver:	n/a	chr12:121342198-121342211 chr12:121341911-121341927 chr12:121342200-121342209 chr12:121342217-121342230 chr12:121341902-121341918 chr12:121341908-121341924 chr12:121341919-121341935 chr12:121342200-121342209 chr12:121342218-121342227 chr12:121342199-121342208 chr12:121342326-121342342 chr12:121341907-121341923 chr12:121341951-121341967 chr12:121342201-121342210 chr12:121342194-121342215 chr12:121342213-121342234
19	BHLHE40	chr12:121344907-121345224	HepG2	liver:	n/a	n/a
20	BHLHE40	chr12:121342103-121342318	HepG2	liver:	n/a	chr12:121342198-121342211 chr12:121342200-121342209 chr12:121342217-121342230 chr12:121342200-121342209 chr12:121342218-121342227 chr12:121342199-121342208 chr12:121342201-121342210 chr12:121342194-121342215 chr12:121342213-121342234
21	BHLHE40	chr12:121342084-121342410	HepG2	liver:	n/a	chr12:121342198-121342211 chr12:121342200-121342209 chr12:121342217-121342230 chr12:121342200-121342209 chr12:121342218-121342227 chr12:121342199-121342208 chr12:121342326-121342342 chr12:121342201-121342210 chr12:121342194-121342215 chr12:121342213-121342234
22	BHLHE40	chr12:121341996-121342663	K562	blood:	n/a	chr12:121342198-121342211 chr12:121342200-121342209 chr12:121342217-121342230 chr12:121342200-121342209 chr12:121342218-121342227 chr12:121342199-121342208 chr12:121342326-121342342 chr12:121342201-121342210 chr12:121342194-121342215 chr12:121342213-121342234
23	BHLHE40	chr12:121341759-121341784	K562	blood:	n/a	n/a
24	BRCA1	chr12:121342109-121342323	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr12:121342129-121342403	HepG2	liver:	n/a	n/a
26	BRCA1	chr12:121342210-121342373	GM12878	blood:	n/a	n/a
27	CBX3	chr12:121355630-121355895	K562	blood:	n/a	n/a
28	CBX3	chr12:121355508-121355968	HCT-116	colon:	n/a	n/a
29	CBX3	chr12:121342027-121342954	K562	blood:	n/a	n/a
30	CCNT2	chr12:121341644-121342532	K562	blood:	n/a	chr12:121342234-121342243 chr12:121342169-121342178 chr12:121342163-121342172
31	CEBPB	chr12:121345698-121345993	IMR90	lung:	n/a	chr12:121345826-121345837
32	CEBPB	chr12:121345777-121345895	HepG2	liver:	n/a	chr12:121345826-121345837
33	CEBPB	chr12:121346198-121346319	HepG2	liver:	n/a	chr12:121346256-121346267 chr12:121346257-121346268 chr12:121346256-121346269
34	CEBPB	chr12:121346198-121346398	HepG2	liver:	n/a	chr12:121346256-121346267 chr12:121346257-121346268 chr12:121346256-121346269
35	CEBPB	chr12:121345792-121345844	K562	blood:	n/a	chr12:121345826-121345837
36	CEBPB	chr12:121345681-121345993	Hela-S3	cervix:	n/a	chr12:121345826-121345837
37	CEBPB	chr12:121345606-121345806	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr12:121342118-121342306	Hela-S3	cervix:	n/a	n/a
39	CEBPD	chr12:121342053-121342630	K562	blood:	n/a	n/a
40	CEBPD	chr12:121342025-121342314	HepG2	liver:	n/a	n/a
41	CEBPD	chr12:121341902-121342399	HepG2	liver:	n/a	n/a
42	CHD1	chr12:121341549-121341864	GM12878	blood:	n/a	n/a
43	CHD2	chr12:121342114-121342600	HepG2	liver:	n/a	chr12:121342232-121342242
44	CHD2	chr12:121341283-121341610	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr12:121341948-121342434	Hela-S3	cervix:	n/a	chr12:121342232-121342242
46	CHD2	chr12:121341216-121341587	GM12878	blood:	n/a	n/a
47	CHD2	chr12:121342111-121342654	K562	blood:	n/a	chr12:121342232-121342242
48	CHD2	chr12:121342155-121342607	H1-hESC	embryonic stem cell:	n/a	chr12:121342232-121342242
49	CHD2	chr12:121342025-121342547	GM12878	blood:	n/a	chr12:121342232-121342242
50	CREB1	chr12:121341075-121342607	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121342321-121342371	AG09309	skin:	n/a
2	chr12:121342321-121342371	AG09309	skin:	n/a
3	chr12:121343033-121343083	SAEC	small airway:	n/a
4	chr12:121342288-121342338	HCF	heart:	n/a
5	chr12:121342321-121342371	NB4	blood:	n/a
6	chr12:121345228-121345278	Caco-2	colon:	n/a
7	chr12:121342288-121342338	GM06990	blood:	n/a
8	chr12:121342288-121342338	HNPCEpiC	eye:	n/a
9	chr12:121342288-121342338	HEK293	kidney:	embryo
10	chr12:121342288-121342338	HAEpiC	amniotic membrane:	n/a
11	chr12:121342288-121342338	NHBE	bronchial:	n/a
12	chr12:121341782-121341832	CMK	blood:	n/a
13	chr12:121342435-121342485	HNPCEpiC	eye:	n/a
14	chr12:121342197-121342247	IMR90	lung:	fetal
15	chr12:121342433-121342483	HCM	heart:	n/a
16	chr12:121341616-121341666	HepG2	liver:	n/a
17	chr12:121345228-121345278	Hela-S3	cervix:	n/a
18	chr12:121341782-121341832	MCF-7	breast:	n/a
19	chr12:121343033-121343083	BJ	skin:	n/a
20	chr12:121342435-121342485	GM19239	blood:	n/a
21	chr12:121341782-121341832	SK-N-SH	brain:	n/a
22	chr12:121345228-121345278	GM12878	blood:	n/a
23	chr12:121341782-121341832	GM12878	blood:	n/a
24	chr12:121342288-121342338	HepG2	liver:	n/a
25	chr12:121345228-121345278	T-47D	breast:	n/a
26	chr12:121341782-121341832	HCF	heart:	n/a
27	chr12:121342197-121342247	AG09319	gingival:	n/a
28	chr12:121342321-121342371	HUVEC	blood vessel:	n/a
29	chr12:121341616-121341666	Hela-S3	cervix:	n/a
30	chr12:121342435-121342485	ovcar-3	ovarian:	n/a
31	chr12:121341616-121341666	H1-hESC	embryonic stem cell:	embryo
32	chr12:121342321-121342371	U87	brain:	n/a
33	chr12:121341782-121341832	A549	lung:	n/a
34	chr12:121342197-121342247	ECC-1	luminal epithelium:	n/a
35	chr12:121345228-121345278	HMEC	breast:	n/a
36	chr12:121342435-121342485	H1-hESC	embryonic stem cell:	embryo
37	chr12:121342433-121342483	GM19239	blood:	n/a
38	chr12:121342433-121342483	GM12892	blood:	n/a
39	chr12:121341782-121341832	AG04450	lung:	fetal
40	chr12:121341616-121341666	SAEC	small airway:	n/a
41	chr12:121341782-121341832	NT2-D1	testis:	n/a
42	chr12:121342197-121342247	BE2_C	brain:	n/a
43	chr12:121342321-121342371	AG04450	lung:	fetal
44	chr12:121342435-121342485	A549	lung:	n/a
45	chr12:121342435-121342485	PANC-1	pancreas:	n/a
46	chr12:121345228-121345278	Hepatocyte	liver:	n/a
47	chr12:121342288-121342338	ECC-1	luminal epithelium:	n/a
48	chr12:121345228-121345278	PFSK-1	brain:	n/a
49	chr12:121342433-121342483	A549	lung:	n/a
50	chr12:121345228-121345278	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:121341147..121344429-chr12:121344566..121350516,5	K562	blood:
2	chr12:121341251..121344109-chr12:121345996..121349521,4	K562	blood:
3	chr12:121339867..121343058-chr12:121346216..121349525,3	MCF-7	breast:
4	chr12:121341724..121342252-chr6:13615154..13615782,2	Hela-S3	cervix:
5	chr12:121336041..121337901-chr12:121343531..121346196,2	MCF-7	breast:
6	chr12:121342121..121344461-chr12:121350958..121352582,2	K562	blood:
7	chr12:121341042..121343632-chr12:121354803..121357357,2	MCF-7	breast:
8	chr12:121342121..121344461-chr12:121350958..121352582,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNF1A-1	chr12:121345458-121345743	XLOC_009911
2	lnc-HNF1A-1	chr12:121342501-121342575	XLOC_009911
3	lnc-HNF1A-1	chr12:121345458-121345743	XLOC_009911
4	lnc-HNF1A-1	chr12:121345458-121345803	XLOC_009911
5	lnc-HNF1A-1	chr12:121342520-121342549	XLOC_009911
6	lnc-HNF1A-1	chr12:121342728-121342811	XLOC_009911

Variant related genes	Relation type
RPL12P33	TF binding region
CLIC1P1	TF binding region
SPPL3	TF binding region
RPL12P33	CpG island
CLIC1P1	CpG island
SPPL3	CpG island
ENSG00000225921	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000157837	chromatin interactions
ENSG00000231313	chromatin interactions
RNF6	miRNA target sites
UBE2E2	miRNA target sites

Extended variants
information (count: 644 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:644 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113043553	chr12:121341583-121341584	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs7966217	chr12:121341586-121341587	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs373570995	chr12:121341640-121341641	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs11610731	chr12:121341736-121341737	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs558783285	chr12:121341756-121341757	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs7966446	chr12:121341762-121341763	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
7	rs567539889	chr12:121341778-121341779	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs11555971	chr12:121341805-121341806	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs541223680	chr12:121341814-121341815	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs2686458	chr12:121341849-121341850	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs11555970	chr12:121341866-121341867	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs2393716	chr12:121341933-121341934	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs543480285	chr12:121341955-121341956	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs188499441	chr12:121342031-121342032	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs532372288	chr12:121342058-121342059	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs552510611	chr12:121342067-121342068	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs904628	chr12:121342084-121342085	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs537885659	chr12:121342141-121342142	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs192784397	chr12:121342146-121342147	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs548387128	chr12:121342156-121342157	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs568089182	chr12:121342158-121342159	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs139706648	chr12:121342166-121342167	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs550369612	chr12:121342181-121342182	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs570435735	chr12:121342196-121342197	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs111323638	chr12:121342199-121342200	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs572440310	chr12:121342219-121342220	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs539016410	chr12:121342308-121342309	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs535155301	chr12:121342328-121342329	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566024973	chr12:121342347-121342348	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs534921990	chr12:121342374-121342375	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554721725	chr12:121342379-121342380	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs35386440	chr12:121342387-121342388	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs183186042	chr12:121342444-121342445	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115169359	chr12:121342489-121342490	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs375556898	chr12:121342495-121342496	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs557137122	chr12:121342557-121342558	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs369221682	chr12:121342588-121342589	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs76032731	chr12:121342734-121342735	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs572271247	chr12:121342773-121342774	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs186926090	chr12:121342797-121342798	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs546208714	chr12:121342850-121342851	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs114442281	chr12:121342853-121342854	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144368708	chr12:121342867-121342868	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542113964	chr12:121342891-121342892	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs7306083	chr12:121342950-121342951	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530578106	chr12:121342977-121342978	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs145265567	chr12:121343017-121343018	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs550652068	chr12:121343072-121343073	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs373475157	chr12:121343113-121343114	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs532806284	chr12:121343167-121343168	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121340000-121342400	Active TSS	H1 Cell Line	embryonic stem cell
2	chr12:121340000-121342400	Active TSS	Fetal Intestine Large	intestine
3	chr12:121340000-121342800	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr12:121340000-121342800	Active TSS	NHDF-Ad	bronchial
5	chr12:121340200-121342600	Active TSS	NHLF	lung
6	chr12:121340200-121343000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr12:121340400-121342200	Active TSS	Colonic Mucosa	Colon
8	chr12:121340400-121342400	Active TSS	H9 Cell Line	embryonic stem cell
9	chr12:121340400-121342400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr12:121340400-121342400	Active TSS	Esophagus	oesophagus
11	chr12:121340400-121342600	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr12:121340400-121342600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:121340400-121342800	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr12:121340400-121343000	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr12:121340600-121341800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
16	chr12:121340600-121342200	Active TSS	HMEC	breast
17	chr12:121340600-121342400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr12:121340600-121342400	Active TSS	Aorta	Aorta
19	chr12:121340600-121342400	Active TSS	Fetal Intestine Small	intestine
20	chr12:121340600-121342400	Active TSS	Lung	lung
21	chr12:121340600-121342400	Active TSS	GM12878-XiMat	blood
22	chr12:121340600-121342600	Active TSS	Duodenum Smooth Muscle	Duodenum
23	chr12:121340600-121342800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr12:121340600-121342800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr12:121340600-121342800	Active TSS	Brain Angular Gyrus	brain
26	chr12:121340600-121342800	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr12:121340600-121342800	Active TSS	HSMM	muscle
28	chr12:121340600-121343000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:121340800-121342200	Active TSS	Placenta	Placenta
30	chr12:121340800-121342400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:121340800-121342400	Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr12:121340800-121342400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:121340800-121342400	Active TSS	Brain Anterior Caudate	brain
34	chr12:121340800-121342400	Active TSS	Duodenum Mucosa	Duodenum
35	chr12:121340800-121342400	Active TSS	Fetal Lung	lung
36	chr12:121340800-121342400	Active TSS	Sigmoid Colon	Sigmoid Colon
37	chr12:121340800-121342400	Active TSS	Thymus	Thymus
38	chr12:121340800-121342400	Active TSS	Spleen	Spleen
39	chr12:121340800-121342400	Active TSS	NHEK	skin
40	chr12:121340800-121342400	Active TSS	Osteobl	bone
41	chr12:121340800-121342600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:121340800-121342600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:121340800-121342600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr12:121340800-121342600	Active TSS	Brain Cingulate Gyrus	brain
45	chr12:121340800-121342600	Active TSS	Brain Substantia Nigra	brain
46	chr12:121340800-121342600	Active TSS	Gastric	stomach
47	chr12:121340800-121342600	Active TSS	Ovary	ovary
48	chr12:121340800-121342600	Active TSS	HSMMtube	muscle
49	chr12:121340800-121342800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr12:121340800-121342800	Active TSS	HUES48 Cell Line	embryonic stem cell

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