Variant report

Variant	esv3393724
Chromosome Location	chr2:133427132-133429630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:365)
CpG islands
(count:794)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:133427676-133428034	H1-hESC	embryonic stem cell:	n/a	chr2:133427843-133427852
2	BACH1	chr2:133427028-133427188	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:133428718-133428793	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr2:133429294-133429379	A549	lung:	n/a	n/a
5	CEBPB	chr2:133428334-133428645	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:133427479-133427827	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr2:133429137-133429391	IMR90	lung:	n/a	chr2:133429153-133429165
8	CEBPB	chr2:133429099-133429422	ECC-1	luminal epithelium:	n/a	chr2:133429153-133429165
9	CEBPB	chr2:133429067-133429427	Hela-S3	cervix:	n/a	chr2:133429153-133429165
10	CHD2	chr2:133427725-133427925	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr2:133428162-133428485	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr2:133429151-133429365	Hela-S3	cervix:	n/a	n/a
13	CTBP2	chr2:133426895-133429093	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:133428756-133428884	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr2:133427000-133427150	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr2:133427000-133427150	HUVEC	blood vessel:	n/a	n/a
17	CTCF	chr2:133426940-133427192	MCF-7	breast:	n/a	n/a
18	CTCF	chr2:133427580-133427730	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr2:133428783-133428854	MCF-7	breast:	n/a	n/a
20	CTCF	chr2:133428900-133429050	AG04450	lung:	n/a	n/a
21	CTCF	chr2:133428381-133428552	NHEK	skin:	n/a	chr2:133428454-133428467
22	CTCF	chr2:133428361-133428507	Fibrobl	skin:	n/a	chr2:133428454-133428467
23	CTCF	chr2:133428412-133428489	ProgFib	skin:	n/a	chr2:133428454-133428467
24	CTCF	chr2:133427040-133427190	MCF-7	breast:	n/a	n/a
25	CTCF	chr2:133428400-133428550	NHEK	skin:	n/a	chr2:133428454-133428467
26	CTCF	chr2:133428375-133428552	Gliobla	brain:	n/a	chr2:133428454-133428467
27	CTCF	chr2:133428520-133428670	HRE	kidney:	n/a	n/a
28	CTCF	chr2:133428420-133428570	Caco-2	colon:	n/a	chr2:133428454-133428467
29	CTCF	chr2:133428400-133428550	AG04449	skin:	n/a	chr2:133428454-133428467
30	CTCF	chr2:133427040-133427190	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr2:133427020-133427170	GM12872	blood:	n/a	n/a
32	CTCF	chr2:133428640-133428790	HRE	kidney:	n/a	n/a
33	CTCF	chr2:133428340-133428490	GM12869	blood:	n/a	chr2:133428454-133428467
34	CTCF	chr2:133427000-133427150	GM12874	blood:	n/a	n/a
35	CTCF	chr2:133427000-133427150	Caco-2	colon:	n/a	n/a
36	CTCF	chr2:133428391-133428511	Hela-S3	cervix:	n/a	chr2:133428454-133428467
37	CTCF	chr2:133428359-133428568	MCF-7	breast:	n/a	chr2:133428454-133428467
38	CTCF	chr2:133426942-133427257	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr2:133428400-133428550	HUVEC	blood vessel:	n/a	chr2:133428454-133428467
40	CTCF	chr2:133428440-133428590	HEK293	kidney:	n/a	chr2:133428454-133428467
41	CTCF	chr2:133426956-133427201	Fibrobl	skin:	n/a	n/a
42	CTCF	chr2:133426924-133427218	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:133427020-133427170	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:133428460-133428610	GM12873	blood:	n/a	n/a
45	CTCF	chr2:133428340-133428490	AG09309	skin:	n/a	chr2:133428454-133428467
46	CTCF	chr2:133427340-133427490	RPTEC	kidney:	n/a	n/a
47	CTCF	chr2:133428320-133428470	SK-N-SH_RA	brain:	n/a	chr2:133428454-133428467
48	CTCF	chr2:133428620-133428770	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr2:133428400-133428550	BJ	skin:	n/a	chr2:133428454-133428467
50	CTCF	chr2:133428251-133428574	MCF-7	breast:	n/a	chr2:133428454-133428467

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:133428652-133428702	BE2_C	brain:	n/a
2	chr2:133428652-133428702	BE2_C	brain:	n/a
3	chr2:133427427-133427477	HL-60	blood:	n/a
4	chr2:133427612-133427662	HCT-116	colon:	n/a
5	chr2:133428993-133429043	CMK	blood:	n/a
6	chr2:133428510-133428560	HNPCEpiC	eye:	n/a
7	chr2:133429169-133429219	HEEpiC	esophagus:	n/a
8	chr2:133428836-133428886	NT2-D1	testis:	n/a
9	chr2:133428422-133428472	AG10803	skin:	n/a
10	chr2:133429169-133429219	HL-60	blood:	n/a
11	chr2:133428422-133428472	BJ	skin:	n/a
12	chr2:133427813-133427863	U87	brain:	n/a
13	chr2:133427813-133427863	GM19239	blood:	n/a
14	chr2:133428502-133428552	T-47D	breast:	n/a
15	chr2:133428422-133428472	HCM	heart:	n/a
16	chr2:133427427-133427477	PANC-1	pancreas:	n/a
17	chr2:133429088-133429138	GM12878	blood:	n/a
18	chr2:133428510-133428560	RPTEC	kidney:	n/a
19	chr2:133429088-133429138	NHBE	bronchial:	n/a
20	chr2:133427427-133427477	HMEC	breast:	n/a
21	chr2:133429088-133429138	GM06990	blood:	n/a
22	chr2:133428422-133428472	H1-hESC	embryonic stem cell:	embryo
23	chr2:133428836-133428886	HCT-116	colon:	n/a
24	chr2:133428836-133428886	HRPEpiC	eye:	n/a
25	chr2:133428993-133429043	HEK293	kidney:	embryo
26	chr2:133427813-133427863	HNPCEpiC	eye:	n/a
27	chr2:133428652-133428702	HMEC	breast:	n/a
28	chr2:133429088-133429138	AG09319	gingival:	n/a
29	chr2:133428510-133428560	Hepatocyte	liver:	n/a
30	chr2:133428510-133428560	HEEpiC	esophagus:	n/a
31	chr2:133427427-133427477	NB4	blood:	n/a
32	chr2:133428652-133428702	U87	brain:	n/a
33	chr2:133427612-133427662	SK-N-MC	brain:	n/a
34	chr2:133428652-133428702	Hepatocyte	liver:	n/a
35	chr2:133429299-133429349	HEEpiC	esophagus:	n/a
36	chr2:133427612-133427662	GM12878	blood:	n/a
37	chr2:133429299-133429349	AG09319	gingival:	n/a
38	chr2:133427427-133427477	RPTEC	kidney:	n/a
39	chr2:133429169-133429219	SAEC	small airway:	n/a
40	chr2:133428836-133428886	ECC-1	luminal epithelium:	n/a
41	chr2:133428993-133429043	ProgFib	skin:	n/a
42	chr2:133429169-133429219	GM19239	blood:	n/a
43	chr2:133428510-133428560	AG10803	skin:	n/a
44	chr2:133428510-133428560	ovcar-3	ovarian:	n/a
45	chr2:133428510-133428560	BE2_C	brain:	n/a
46	chr2:133429088-133429138	T-47D	breast:	n/a
47	chr2:133428523-133428573	NB4	blood:	n/a
48	chr2:133428993-133429043	HCM	heart:	n/a
49	chr2:133427612-133427662	Jurkat	blood:	n/a
50	chr2:133427612-133427662	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr2:133173744..133175513-chr2:133427199..133429009,2	MCF-7	breast:
2	chr2:133428080..133428797-chr2:133928852..133929367,2	MCF-7	breast:
3	chr2:133395862..133396428-chr2:133427987..133428958,2	MCF-7	breast:

No data

Variant related genes	Relation type
LYPD1	TF binding region
LYPD1	CpG island
ENSG00000183840	chromatin interactions

Extended variants
information (count: 89 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7608736	chr2:133427151-133427152	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554414780	chr2:133427293-133427294	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543449447	chr2:133427295-133427296	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs71413517	chr2:133427297-133427298	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs576686247	chr2:133427312-133427313	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs544002815	chr2:133427315-133427316	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs191331100	chr2:133427343-133427344	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577424444	chr2:133427380-133427381	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375755999	chr2:133427393-133427394	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs370451698	chr2:133427403-133427404	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374586388	chr2:133427410-133427411	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368126044	chr2:133427423-133427424	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs546751159	chr2:133427425-133427426	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370933172	chr2:133427430-133427431	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375699371	chr2:133427433-133427434	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535269409	chr2:133427438-133427439	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs368596177	chr2:133427439-133427440	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368512774	chr2:133427464-133427465	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs372984166	chr2:133427473-133427474	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376496582	chr2:133427488-133427489	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs367807018	chr2:133427510-133427511	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371451824	chr2:133427512-133427513	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs559083376	chr2:133427531-133427532	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375773838	chr2:133427533-133427534	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376036521	chr2:133427543-133427544	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184607068	chr2:133427583-133427584	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs541502777	chr2:133427589-133427590	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs563016686	chr2:133427600-133427601	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs114525740	chr2:133427604-133427605	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551914471	chr2:133427655-133427656	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570630760	chr2:133427663-133427664	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs528374856	chr2:133427670-133427671	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558587805	chr2:133427671-133427672	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs11415586	chr2:133427696-133427697	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs546917896	chr2:133427708-133427709	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs565923118	chr2:133427726-133427727	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536670206	chr2:133427787-133427788	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs111860298	chr2:133427871-133427872	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs570128309	chr2:133427888-133427889	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs537549908	chr2:133427971-133427972	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs369162146	chr2:133427973-133427974	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs553894818	chr2:133427990-133427991	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs371745453	chr2:133428003-133428004	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs558837163	chr2:133428067-133428068	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189271928	chr2:133428080-133428081	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs74937389	chr2:133428093-133428094	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs553657705	chr2:133428122-133428123	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs112775610	chr2:133428211-133428212	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs574814761	chr2:133428219-133428220	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs541392158	chr2:133428241-133428242	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17621639	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21509527	CNVD
Mental retardation	17124404	CNVD
Colorectal cancer	20459617	CNVD
Neuroticism	17667963	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:133425400-133429200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
2	chr2:133425600-133427200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:133425600-133427600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:133425800-133427600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:133425800-133429000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
6	chr2:133425800-133429200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
7	chr2:133425800-133429200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
8	chr2:133425800-133429200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:133425800-133429200	Active TSS	Fetal Kidney	kidney
10	chr2:133426000-133427200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
11	chr2:133426000-133427600	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
12	chr2:133426000-133427600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
13	chr2:133426000-133427600	Bivalent Enhancer	Placenta	Placenta
14	chr2:133426000-133427600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
15	chr2:133426000-133428200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:133426000-133428200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:133426000-133428800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
18	chr2:133426000-133428800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
19	chr2:133426000-133429000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr2:133426000-133429000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:133426000-133429000	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
22	chr2:133426000-133429200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
23	chr2:133426000-133429400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
24	chr2:133426000-133429400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
25	chr2:133426200-133427600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
26	chr2:133426200-133428000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
27	chr2:133426200-133428800	Active TSS	Brain Anterior Caudate	brain
28	chr2:133426400-133427200	Bivalent/Poised TSS	NHLF	lung
29	chr2:133426400-133428000	Active TSS	Fetal Brain Female	brain
30	chr2:133426400-133428400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:133426400-133429000	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr2:133426600-133427200	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
33	chr2:133426600-133427200	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
34	chr2:133426600-133427200	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
35	chr2:133426600-133427400	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:133426600-133427400	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
37	chr2:133426600-133427400	Flanking Active TSS	Ovary	ovary
38	chr2:133426600-133427400	Flanking Bivalent TSS/Enh	Osteobl	bone
39	chr2:133426600-133427600	Flanking Active TSS	Pancreas	Pancrea
40	chr2:133426600-133427800	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr2:133426600-133428600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:133426600-133428600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr2:133426600-133428600	Flanking Bivalent TSS/Enh	NHEK	skin
44	chr2:133426600-133428800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:133426600-133428800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr2:133426600-133429000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
47	chr2:133426600-133429000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
48	chr2:133426600-133429000	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
49	chr2:133426600-133429000	Bivalent Enhancer	Spleen	Spleen
50	chr2:133426600-133429200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin

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