Variant report

Variant	nsv961427
Chromosome Location	chr2:87032925-87059989
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	chr2:87035534-87035903	K562	blood:	n/a	n/a
2	ARID3A	chr2:87035044-87036047	HepG2	liver:	n/a	n/a
3	ATF1	chr2:87046445-87047301	K562	blood:	n/a	n/a
4	ATF1	chr2:87056647-87057105	K562	blood:	n/a	n/a
5	ATF3	chr2:87035407-87035871	A549	lung:	n/a	n/a
6	ATF3	chr2:87035386-87035875	A549	lung:	n/a	n/a
7	BACH1	chr2:87035036-87035962	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr2:87059079-87059327	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr2:87035400-87035852	GM12878	blood:	n/a	chr2:87035834-87035847
10	BCLAF1	chr2:87035432-87035863	GM12878	blood:	n/a	chr2:87035834-87035847
11	BHLHE40	chr2:87035439-87036253	K562	blood:	n/a	n/a
12	BHLHE40	chr2:87035462-87036013	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:87056607-87056890	K562	blood:	n/a	n/a
14	BHLHE40	chr2:87034191-87035985	HepG2	liver:	n/a	n/a
15	BHLHE40	chr2:87051039-87051340	K562	blood:	n/a	n/a
16	BRCA1	chr2:87059602-87059802	HepG2	liver:	n/a	chr2:87059766-87059773
17	BRCA1	chr2:87052250-87052793	HepG2	liver:	n/a	n/a
18	BRCA1	chr2:87034355-87036171	HepG2	liver:	n/a	n/a
19	BRCA1	chr2:87035437-87036065	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr2:87048502-87048716	GM12878	blood:	n/a	n/a
21	CBX3	chr2:87035466-87035877	K562	blood:	n/a	n/a
22	CEBPB	chr2:87044171-87044813	IMR90	lung:	n/a	n/a
23	CEBPB	chr2:87034289-87034930	MCF-7	breast:	n/a	chr2:87034394-87034405
24	CEBPB	chr2:87035482-87036290	Hela-S3	cervix:	n/a	chr2:87035957-87035974
25	CEBPB	chr2:87035466-87036639	H1-hESC	embryonic stem cell:	n/a	chr2:87035957-87035974
26	CEBPB	chr2:87034262-87034858	HepG2	liver:	n/a	chr2:87034394-87034405
27	CEBPB	chr2:87035699-87036492	HepG2	liver:	n/a	chr2:87035957-87035974
28	CEBPB	chr2:87034280-87034494	HepG2	liver:	n/a	chr2:87034394-87034405
29	CEBPB	chr2:87034146-87036421	A549	lung:	n/a	chr2:87034394-87034405 chr2:87035957-87035974
30	CEBPD	chr2:87035566-87036164	K562	blood:	n/a	n/a
31	CHD2	chr2:87035285-87036007	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr2:87052689-87053040	HepG2	liver:	n/a	n/a
33	CHD2	chr2:87034544-87035946	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr2:87034496-87036015	HepG2	liver:	n/a	n/a
35	CHD2	chr2:87035510-87035972	K562	blood:	n/a	n/a
36	CREB1	chr2:87034492-87034903	A549	lung:	n/a	n/a
37	CREB1	chr2:87034934-87035865	A549	lung:	n/a	n/a
38	CTCF	chr2:87035560-87035710	MCF-7	breast:	n/a	chr2:87035650-87035671 chr2:87035653-87035663 chr2:87035648-87035666 chr2:87035651-87035660 chr2:87035651-87035664
39	CTCF	chr2:87035600-87035750	AG09309	skin:	n/a	chr2:87035650-87035671 chr2:87035653-87035663 chr2:87035648-87035666 chr2:87035651-87035660 chr2:87035651-87035664
40	CTCF	chr2:87035487-87035833	MCF-7	breast:	n/a	chr2:87035650-87035671 chr2:87035653-87035663 chr2:87035648-87035666 chr2:87035551-87035559 chr2:87035651-87035660 chr2:87035651-87035664
41	CTCF	chr2:87035509-87035769	HUVEC	blood vessel:	n/a	chr2:87035650-87035671 chr2:87035653-87035663 chr2:87035648-87035666 chr2:87035551-87035559 chr2:87035651-87035660 chr2:87035651-87035664
42	CTCF	chr2:87034601-87034958	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:87035488-87035841	Gliobla	brain:	n/a	chr2:87035650-87035671 chr2:87035653-87035663 chr2:87035648-87035666 chr2:87035551-87035559 chr2:87035651-87035660 chr2:87035651-87035664
44	CTCF	chr2:87035880-87036030	HCM	heart:	n/a	n/a
45	CTCF	chr2:87035479-87035814	NHEK	skin:	n/a	chr2:87035650-87035671 chr2:87035653-87035663 chr2:87035648-87035666 chr2:87035551-87035559 chr2:87035651-87035660 chr2:87035651-87035664
46	CTCF	chr2:87034480-87034630	Caco-2	colon:	n/a	n/a
47	CTCF	chr2:87034743-87034824	GM13977	blood:	n/a	n/a
48	CTCF	chr2:87034719-87034925	GM12891	blood:	n/a	n/a
49	CTCF	chr2:87034662-87034890	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:87035580-87035730	GM12878	blood:	n/a	chr2:87035650-87035671 chr2:87035653-87035663 chr2:87035648-87035666 chr2:87035651-87035660 chr2:87035651-87035664

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:87052406-87052456	Hela-S3	cervix:	n/a
2	chr2:87052406-87052456	Hela-S3	cervix:	n/a
3	chr2:87036626-87036676	ECC-1	luminal epithelium:	n/a
4	chr2:87037000-87037050	ovcar-3	ovarian:	n/a
5	chr2:87037038-87037088	MCF-7	breast:	n/a
6	chr2:87035688-87035738	T-47D	breast:	n/a
7	chr2:87034831-87034881	NHDF-neo	bronchial:	n/a
8	chr2:87035716-87035766	LNCaP	prostate:	n/a
9	chr2:87035278-87035328	NT2-D1	testis:	n/a
10	chr2:87059202-87059252	U87	brain:	n/a
11	chr2:87035698-87035748	Hepatocyte	liver:	n/a
12	chr2:87036948-87036998	HRE	kidney:	n/a
13	chr2:87059202-87059252	CMK	blood:	n/a
14	chr2:87034831-87034881	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:87034200-87034250	Caco-2	colon:	n/a
16	chr2:87059202-87059252	ovcar-3	ovarian:	n/a
17	chr2:87035688-87035738	SK-N-MC	brain:	n/a
18	chr2:87035982-87036032	HRCEpiC	kidney:	n/a
19	chr2:87035716-87035766	HMEC	breast:	n/a
20	chr2:87037000-87037050	PANC-1	pancreas:	n/a
21	chr2:87048747-87048797	GM12892	blood:	n/a
22	chr2:87035278-87035328	HepG2	liver:	n/a
23	chr2:87035758-87035808	HCPEpiC	choroid plexus:	n/a
24	chr2:87035502-87035552	GM12892	blood:	n/a
25	chr2:87035758-87035808	HEEpiC	esophagus:	n/a
26	chr2:87048489-87048539	SK-N-MC	brain:	n/a
27	chr2:87034663-87034713	BJ	skin:	n/a
28	chr2:87048489-87048539	AG04450	lung:	fetal
29	chr2:87037038-87037088	HRCEpiC	kidney:	n/a
30	chr2:87034663-87034713	SKMC	muscle:	n/a
31	chr2:87037000-87037050	SK-N-MC	brain:	n/a
32	chr2:87034800-87034850	HUVEC	blood vessel:	n/a
33	chr2:87037000-87037050	GM12891	blood:	n/a
34	chr2:87034663-87034713	NHDF-neo	bronchial:	n/a
35	chr2:87035698-87035748	RPTEC	kidney:	n/a
36	chr2:87052595-87052645	NT2-D1	testis:	n/a
37	chr2:87035698-87035748	HepG2	liver:	n/a
38	chr2:87035758-87035808	NH-A	brain:	n/a
39	chr2:87034831-87034881	AG09309	skin:	n/a
40	chr2:87035688-87035738	NH-A	brain:	n/a
41	chr2:87037038-87037088	AG04450	lung:	fetal
42	chr2:87034831-87034881	GM12878	blood:	n/a
43	chr2:87035609-87035659	AG10803	skin:	n/a
44	chr2:87036626-87036676	SAEC	small airway:	n/a
45	chr2:87036626-87036676	SK-N-MC	brain:	n/a
46	chr2:87035278-87035328	SK-N-SH	brain:	n/a
47	chr2:87034663-87034713	NT2-D1	testis:	n/a
48	chr2:87059202-87059252	HPAEpiC	pulmonary alveolar:	n/a
49	chr2:87035698-87035748	HL-60	blood:	n/a
50	chr2:87052595-87052645	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:87037113..87040779-chr2:87041789..87043828,3	MCF-7	breast:
2	chr2:86849445..86851190-chr2:87032691..87035125,2	MCF-7	breast:
3	chr2:87016632..87018790-chr2:87032170..87034818,2	MCF-7	breast:
4	chr2:86623288..86624016-chr2:87035607..87036117,2	K562	blood:
5	chr2:87027429..87029598-chr2:87032662..87035467,2	MCF-7	breast:
6	chr2:87035298..87037035-chr2:87037234..87038983,2	MCF-7	breast:
7	chr2:87046936..87049292-chr2:87052783..87055158,2	K562	blood:
8	chr2:86991626..86993002-chr2:87034779..87035758,6	MCF-7	breast:
9	chr2:87030047..87032736-chr2:87033123..87034744,3	MCF-7	breast:
10	chr2:87053953..87055906-chr2:87062095..87066104,3	MCF-7	breast:
11	chr2:87046936..87049292-chr2:87052783..87055158,2	K562	blood:
12	chr2:87037113..87040779-chr2:87041789..87043828,3	MCF-7	breast:

Variant related genes	Relation type
CD8A	TF binding region
CD8A	CpG island
ENSG00000239305	chromatin interactions
ENSG00000153563	chromatin interactions
ENSG00000249884	chromatin interactions
ENSG00000153561	chromatin interactions

Extended variants
information (count: 973 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145648580	chr2:87032945-87032946	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs569937111	chr2:87032973-87032974	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs369121870	chr2:87032981-87032982	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs192903033	chr2:87033006-87033007	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs185459872	chr2:87033008-87033009	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs554857985	chr2:87033019-87033020	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs534949700	chr2:87033023-87033024	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs75506306	chr2:87033033-87033034	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs148473179	chr2:87033036-87033037	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs142621750	chr2:87033040-87033041	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546923054	chr2:87033043-87033044	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs555767455	chr2:87033053-87033054	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs556650704	chr2:87033063-87033064	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs144436714	chr2:87033065-87033066	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs190027538	chr2:87033066-87033067	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs373310709	chr2:87033068-87033069	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs565463453	chr2:87033069-87033070	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs539130100	chr2:87033074-87033075	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs557371091	chr2:87033116-87033117	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs181773916	chr2:87033152-87033153	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs370480889	chr2:87033171-87033172	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs571199530	chr2:87033340-87033341	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs537751898	chr2:87033365-87033366	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs377652870	chr2:87033374-87033375	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs186509941	chr2:87033387-87033388	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs538302621	chr2:87033389-87033390	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs559965194	chr2:87033514-87033515	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs578170173	chr2:87033540-87033541	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs545511312	chr2:87033549-87033550	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs146472624	chr2:87033557-87033558	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs114320823	chr2:87033592-87033593	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs550062417	chr2:87033639-87033640	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs188155581	chr2:87033682-87033683	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs6754318	chr2:87033686-87033687	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547222469	chr2:87033719-87033720	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs78693623	chr2:87033724-87033725	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs76486294	chr2:87033729-87033730	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs551014735	chr2:87033733-87033734	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs73947270	chr2:87033758-87033759	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs536609196	chr2:87033842-87033843	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs556048685	chr2:87033882-87033883	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs371210326	chr2:87033886-87033887	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs368069376	chr2:87033997-87033998	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs115789387	chr2:87034008-87034009	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs535321718	chr2:87034038-87034039	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs553645815	chr2:87034175-87034176	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2367375	chr2:87034294-87034295	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs114837321	chr2:87034316-87034317	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs180991291	chr2:87034391-87034392	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs575613794	chr2:87034393-87034394	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:87024600-87033200	Weak transcription	Primary T cells from cord blood	blood
2	chr2:87032200-87033800	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr2:87032400-87033000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr2:87032400-87033000	Flanking Active TSS	Thymus	Thymus
5	chr2:87032600-87033200	Enhancers	Primary T cells fromperipheralblood	blood
6	chr2:87032800-87033200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr2:87032800-87033200	Active TSS	Fetal Thymus	thymus
8	chr2:87032800-87034400	Weak transcription	Right Atrium	heart
9	chr2:87033000-87033200	Active TSS	Thymus	Thymus
10	chr2:87033000-87033600	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr2:87033200-87033400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr2:87033200-87033400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
13	chr2:87033200-87033800	Transcr. at gene 5' and 3'	Thymus	Thymus
14	chr2:87033200-87034200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr2:87033200-87034600	Flanking Active TSS	Fetal Thymus	thymus
16	chr2:87033200-87034800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
17	chr2:87033200-87035000	Active TSS	Primary T cells from cord blood	blood
18	chr2:87033400-87033600	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
19	chr2:87033400-87033600	Enhancers	Esophagus	oesophagus
20	chr2:87033400-87034200	Bivalent Enhancer	Placenta	Placenta
21	chr2:87033600-87033800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
22	chr2:87033600-87034000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:87033600-87034000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr2:87033600-87034000	Flanking Bivalent TSS/Enh	HepG2	liver
25	chr2:87033600-87034400	Enhancers	Brain Angular Gyrus	brain
26	chr2:87033600-87034600	Weak transcription	Esophagus	oesophagus
27	chr2:87033600-87034600	Enhancers	Spleen	Spleen
28	chr2:87033800-87034000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
29	chr2:87033800-87034000	Enhancers	Fetal Brain Male	brain
30	chr2:87033800-87034000	Bivalent Enhancer	Fetal Brain Female	brain
31	chr2:87033800-87034000	Flanking Active TSS	Thymus	Thymus
32	chr2:87033800-87034400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr2:87033800-87034600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr2:87034000-87034200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:87034000-87034200	Flanking Active TSS	Fetal Brain Female	brain
36	chr2:87034000-87034200	Bivalent Enhancer	HepG2	liver
37	chr2:87034000-87034400	Weak transcription	Fetal Brain Male	brain
38	chr2:87034000-87034400	Enhancers	Fetal Heart	heart
39	chr2:87034000-87034600	Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr2:87034000-87037000	Active TSS	Thymus	Thymus
41	chr2:87034000-87037400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
42	chr2:87034200-87034400	Enhancers	Primary hematopoietic stem cells	blood
43	chr2:87034200-87034400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
44	chr2:87034200-87034400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr2:87034200-87034400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:87034200-87034400	Enhancers	Fetal Intestine Large	intestine
47	chr2:87034200-87034400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr2:87034200-87034400	Enhancers	Right Ventricle	heart
49	chr2:87034200-87034400	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr2:87034200-87034400	Bivalent/Poised TSS	HepG2	liver

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