Variant report

Variant	esv3420951
Chromosome Location	chr15:44486085-44488633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:537)
CpG islands
(count:854)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:537 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:44487398-44487636	HepG2	liver:	n/a	n/a
2	BHLHE40	chr15:44487373-44487862	HepG2	liver:	n/a	n/a
3	BHLHE40	chr15:44487368-44487684	A549	lung:	n/a	n/a
4	BHLHE40	chr15:44487395-44487682	GM12878	blood:	n/a	n/a
5	BRCA1	chr15:44487478-44487480	HepG2	liver:	n/a	n/a
6	BRCA1	chr15:44487437-44487846	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr15:44487455-44487861	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr15:44487636-44487867	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr15:44486611-44486722	K562	blood:	n/a	n/a
10	CEBPB	chr15:44486543-44486881	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr15:44486307-44486816	IMR90	lung:	n/a	n/a
12	CEBPZ	chr15:44487425-44487790	HepG2	liver:	n/a	n/a
13	CHD1	chr15:44486909-44487044	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD1	chr15:44487578-44487980	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr15:44487557-44487688	K562	blood:	n/a	n/a
16	CHD2	chr15:44487265-44487971	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr15:44486605-44486999	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr15:44487364-44488027	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr15:44487427-44487839	GM12878	blood:	n/a	n/a
20	CHD2	chr15:44487356-44487808	HepG2	liver:	n/a	n/a
21	CREB1	chr15:44487372-44488023	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr15:44487257-44487827	A549	lung:	n/a	n/a
23	CTCF	chr15:44486720-44486870	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr15:44487620-44487770	HEEpiC	esophagus:	n/a	chr15:44487691-44487701
25	CTCF	chr15:44486700-44486850	NHEK	skin:	n/a	n/a
26	CTCF	chr15:44487600-44487750	SAEC	small airway:	n/a	chr15:44487691-44487701
27	CTCF	chr15:44487600-44487750	HCFaa	heart:	n/a	chr15:44487691-44487701
28	CTCF	chr15:44487620-44487770	AG09309	skin:	n/a	chr15:44487691-44487701
29	CTCF	chr15:44487620-44487770	GM12872	blood:	n/a	chr15:44487691-44487701
30	CTCF	chr15:44487560-44487710	HPAF	blood vessel:	n/a	chr15:44487691-44487701
31	CTCF	chr15:44487600-44487750	WI-38	lung:	n/a	chr15:44487691-44487701
32	CTCF	chr15:44487596-44487700	GM13977	blood:	n/a	n/a
33	CTCF	chr15:44487580-44487730	BJ	skin:	n/a	chr15:44487691-44487701
34	CTCF	chr15:44487580-44487730	A549	lung:	n/a	chr15:44487691-44487701
35	CTCF	chr15:44486800-44486950	RPTEC	kidney:	n/a	n/a
36	CTCF	chr15:44487660-44487810	HMEC	breast:	n/a	chr15:44487691-44487701
37	CTCF	chr15:44487540-44487690	RPTEC	kidney:	n/a	n/a
38	CTCF	chr15:44487580-44487730	GM12864	blood:	n/a	chr15:44487691-44487701
39	CTCF	chr15:44487567-44487837	Fibrobl	skin:	n/a	chr15:44487691-44487701
40	CTCF	chr15:44486840-44486990	GM12868	blood:	n/a	n/a
41	CTCF	chr15:44486700-44486850	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr15:44487536-44487808	GM12891	blood:	n/a	chr15:44487691-44487701
43	CTCF	chr15:44486800-44486950	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr15:44487580-44487730	GM12873	blood:	n/a	chr15:44487691-44487701
45	CTCF	chr15:44487660-44487810	Hela-S3	cervix:	n/a	chr15:44487691-44487701
46	CTCF	chr15:44487588-44487776	ProgFib	skin:	n/a	chr15:44487691-44487701
47	CTCF	chr15:44487600-44487750	HCPEpiC	choroid plexus:	n/a	chr15:44487691-44487701
48	CTCF	chr15:44486660-44486810	GM12873	blood:	n/a	n/a
49	CTCF	chr15:44487560-44487710	NHDF-neo	bronchial:	n/a	chr15:44487691-44487701
50	CTCF	chr15:44486798-44486992	NHEK	skin:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:44487788-44487838	NHDF-neo	bronchial:	n/a
2	chr15:44487924-44487974	HRCEpiC	kidney:	n/a
3	chr15:44487547-44487597	HIPEpiC	eye:	n/a
4	chr15:44487605-44487655	HEK293	kidney:	embryo
5	chr15:44486621-44486671	A549	lung:	n/a
6	chr15:44487547-44487597	HUVEC	blood vessel:	n/a
7	chr15:44486207-44486257	GM12891	blood:	n/a
8	chr15:44487728-44487778	AG09319	gingival:	n/a
9	chr15:44486207-44486257	HMEC	breast:	n/a
10	chr15:44487545-44487595	AG04450	lung:	fetal
11	chr15:44487308-44487358	Hela-S3	cervix:	n/a
12	chr15:44487547-44487597	T-47D	breast:	n/a
13	chr15:44487308-44487358	AG09309	skin:	n/a
14	chr15:44487788-44487838	NT2-D1	testis:	n/a
15	chr15:44486621-44486671	BE2_C	brain:	n/a
16	chr15:44486621-44486671	GM19239	blood:	n/a
17	chr15:44486207-44486257	PANC-1	pancreas:	n/a
18	chr15:44487605-44487655	NHDF-neo	bronchial:	n/a
19	chr15:44486450-44486500	A549	lung:	n/a
20	chr15:44486207-44486257	SK-N-MC	brain:	n/a
21	chr15:44487192-44487242	GM06990	blood:	n/a
22	chr15:44486207-44486257	SKMC	muscle:	n/a
23	chr15:44487292-44487342	GM06990	blood:	n/a
24	chr15:44487308-44487358	Hepatocyte	liver:	n/a
25	chr15:44487547-44487597	HCF	heart:	n/a
26	chr15:44486450-44486500	GM12892	blood:	n/a
27	chr15:44487308-44487358	HNPCEpiC	eye:	n/a
28	chr15:44487788-44487838	AG09319	gingival:	n/a
29	chr15:44487910-44487960	SKMC	muscle:	n/a
30	chr15:44487924-44487974	K562	blood:	n/a
31	chr15:44486562-44486612	Caco-2	colon:	n/a
32	chr15:44487605-44487655	HCM	heart:	n/a
33	chr15:44486450-44486500	ProgFib	skin:	n/a
34	chr15:44487192-44487242	AG09309	skin:	n/a
35	chr15:44487547-44487597	GM12878	blood:	n/a
36	chr15:44487192-44487242	SK-N-SH	brain:	n/a
37	chr15:44486621-44486671	HMEC	breast:	n/a
38	chr15:44486207-44486257	SAEC	small airway:	n/a
39	chr15:44487728-44487778	NH-A	brain:	n/a
40	chr15:44487924-44487974	HCT-116	colon:	n/a
41	chr15:44487547-44487597	GM06990	blood:	n/a
42	chr15:44487910-44487960	NT2-D1	testis:	n/a
43	chr15:44487292-44487342	BE2_C	brain:	n/a
44	chr15:44487545-44487595	AoSMC	blood vessel:	n/a
45	chr15:44486207-44486257	GM12892	blood:	n/a
46	chr15:44487547-44487597	A549	lung:	n/a
47	chr15:44487728-44487778	HCF	heart:	n/a
48	chr15:44487910-44487960	Hepatocyte	liver:	n/a
49	chr15:44487788-44487838	BE2_C	brain:	n/a
50	chr15:44487728-44487778	NB4	blood:	n/a

No data

Variant related genes	Relation type
FRMD5	TF binding region
FRMD5	CpG island

Extended variants
information (count: 88 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:88 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575846527	chr15:44486157-44486158	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs35147214	chr15:44486179-44486180	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2706465	chr15:44486239-44486240	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs570899016	chr15:44486291-44486292	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537286824	chr15:44486310-44486311	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374082461	chr15:44486332-44486333	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546313261	chr15:44486349-44486350	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533466144	chr15:44486356-44486357	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144601956	chr15:44486466-44486467	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2706464	chr15:44486511-44486512	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs555511240	chr15:44486519-44486520	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556116484	chr15:44486579-44486580	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566327776	chr15:44486596-44486597	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535238761	chr15:44486640-44486641	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34524930	chr15:44486674-44486675	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs558321061	chr15:44486677-44486678	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs577711774	chr15:44486772-44486773	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs573955729	chr15:44486775-44486776	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs78549774	chr15:44486786-44486787	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs573325391	chr15:44486788-44486789	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs542171321	chr15:44486831-44486832	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs559232584	chr15:44486856-44486857	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs528361208	chr15:44486874-44486875	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs544853551	chr15:44486884-44486885	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs565072736	chr15:44486921-44486922	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs142483823	chr15:44486958-44486959	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs138760454	chr15:44487052-44487053	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs550262461	chr15:44487062-44487063	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs570022793	chr15:44487076-44487077	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs558409241	chr15:44487100-44487101	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs369076274	chr15:44487114-44487115	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374169698	chr15:44487123-44487124	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs373573756	chr15:44487130-44487131	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs549354619	chr15:44487265-44487266	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs566415910	chr15:44487299-44487300	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs535331870	chr15:44487350-44487351	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs372929275	chr15:44487363-44487364	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs373990283	chr15:44487389-44487390	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs115489154	chr15:44487439-44487440	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs571795271	chr15:44487460-44487461	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs376855236	chr15:44487478-44487479	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs557024482	chr15:44487505-44487506	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573360605	chr15:44487522-44487523	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs186218970	chr15:44487527-44487528	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs552548518	chr15:44487540-44487541	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs374481565	chr15:44487548-44487549	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs536136858	chr15:44487567-44487568	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs190168282	chr15:44487568-44487569	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs182579097	chr15:44487591-44487592	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs73409812	chr15:44487617-44487618	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Mental retardation	17124404	CNVD
Melanoma	17363583	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44484200-44486600	Flanking Active TSS	HUVEC	blood vessel
2	chr15:44484200-44487800	Active TSS	Brain Anterior Caudate	brain
3	chr15:44484200-44488000	Active TSS	Brain Hippocampus Middle	brain
4	chr15:44484200-44488000	Active TSS	Brain Substantia Nigra	brain
5	chr15:44484200-44488200	Active TSS	Brain Inferior Temporal Lobe	brain
6	chr15:44484200-44488200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:44484400-44487800	Active TSS	Brain Angular Gyrus	brain
8	chr15:44484400-44487800	Active TSS	Brain Cingulate Gyrus	brain
9	chr15:44484600-44487600	Active TSS	HMEC	breast
10	chr15:44484600-44488200	Active TSS	Fetal Brain Female	brain
11	chr15:44484600-44488200	Active TSS	NH-A	brain
12	chr15:44484800-44486200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
13	chr15:44484800-44486800	Active TSS	Fetal Brain Male	brain
14	chr15:44485200-44486800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:44485400-44486200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
16	chr15:44485400-44486200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr15:44485400-44486200	Flanking Active TSS	NHEK	skin
18	chr15:44485400-44487000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr15:44485600-44486200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
20	chr15:44485600-44486200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:44485600-44486200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr15:44485600-44486600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr15:44485600-44486600	Bivalent/Poised TSS	NHDF-Ad	bronchial
24	chr15:44485600-44487200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
25	chr15:44485600-44488000	Active TSS	Right Atrium	heart
26	chr15:44485600-44488200	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr15:44485800-44486200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr15:44485800-44486200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
29	chr15:44485800-44486200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr15:44485800-44486200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
31	chr15:44485800-44486200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
32	chr15:44485800-44486200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr15:44485800-44486200	Bivalent Enhancer	Adipose Nuclei	Adipose
34	chr15:44485800-44486200	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr15:44485800-44486200	Enhancers	Gastric	stomach
36	chr15:44485800-44486400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
37	chr15:44485800-44486400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
38	chr15:44485800-44486400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:44485800-44486400	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
40	chr15:44485800-44486400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
41	chr15:44485800-44486400	Flanking Active TSS	NHLF	lung
42	chr15:44485800-44486600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr15:44485800-44486600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
44	chr15:44485800-44486600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr15:44485800-44486600	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
46	chr15:44485800-44486600	Bivalent/Poised TSS	Fetal Heart	heart
47	chr15:44485800-44486800	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:44485800-44486800	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr15:44485800-44486800	Enhancers	Pancreas	Pancrea
50	chr15:44485800-44486800	Flanking Bivalent TSS/Enh	Rectal Smooth Muscle	rectum

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