Variant report

Variant	esv3388771
Chromosome Location	chr15:73659224-73662947
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:58)
CpG islands
(count:732)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:58 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:73660382-73660487	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:73661673-73662017	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr15:73661147-73661495	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr15:73661810-73661950	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr15:73659383-73659628	H1-hESC	embryonic stem cell:	n/a	n/a
6	CREB1	chr15:73660758-73661270	A549	lung:	n/a	n/a
7	CTBP2	chr15:73660453-73662080	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr15:73661660-73661810	HEK293	kidney:	n/a	n/a
9	CTCF	chr15:73659429-73659592	H1-hESC	embryonic stem cell:	n/a	n/a
10	E2F6	chr15:73661598-73662138	H1-hESC	embryonic stem cell:	n/a	n/a
11	E2F6	chr15:73661021-73662142	H1-hESC	embryonic stem cell:	n/a	chr15:73661348-73661358 chr15:73661368-73661377
12	EGR1	chr15:73660750-73661091	H1-hESC	embryonic stem cell:	n/a	chr15:73660850-73660860
13	GABPA	chr15:73659868-73660191	H1-hESC	embryonic stem cell:	n/a	n/a
14	GABPA	chr15:73660218-73660719	H1-hESC	embryonic stem cell:	n/a	n/a
15	HA-E2F1	chr15:73660599-73661316	MCF-7	breast:	n/a	n/a
16	JUN	chr15:73662674-73662725	HepG2	liver:	n/a	chr15:73662684-73662693 chr15:73662683-73662696
17	JUND	chr15:73660801-73660981	H1-hESC	embryonic stem cell:	n/a	n/a
18	JUND	chr15:73661110-73661363	H1-hESC	embryonic stem cell:	n/a	n/a
19	MAX	chr15:73661092-73662035	H1-hESC	embryonic stem cell:	n/a	chr15:73661277-73661286 chr15:73661186-73661195
20	MAX	chr15:73661643-73662133	H1-hESC	embryonic stem cell:	n/a	n/a
21	MXI1	chr15:73660358-73660443	H1-hESC	embryonic stem cell:	n/a	n/a
22	MXI1	chr15:73660738-73661344	H1-hESC	embryonic stem cell:	n/a	chr15:73661277-73661292
23	MXI1	chr15:73661812-73662012	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr15:73660536-73661506	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr15:73660078-73660134	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr15:73660870-73660876	MCF-7	breast:	n/a	n/a
27	POLR2A	chr15:73660880-73661126	MCF-7	breast:	n/a	n/a
28	POLR2A	chr15:73660730-73661394	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr15:73660755-73661299	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr15:73661446-73661976	H1-neurons	neurons:	n/a	n/a
31	POLR2A	chr15:73660132-73660634	H1-neurons	neurons:	n/a	n/a
32	POLR2A	chr15:73660142-73660195	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr15:73661556-73661928	H1-neurons	neurons:	n/a	n/a
34	POLR2A	chr15:73661065-73661066	Gliobla	brain:	n/a	n/a
35	POLR2A	chr15:73659380-73659574	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr15:73660982-73661251	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr15:73661014-73661278	HCT-116	colon:	n/a	n/a
38	POLR2A	chr15:73662634-73662788	GM12878	blood:	n/a	n/a
39	POLR2A	chr15:73660679-73661446	H1-neurons	neurons:	n/a	n/a
40	POLR2A	chr15:73660360-73661393	H1-neurons	neurons:	n/a	n/a
41	RAD21	chr15:73659275-73659771	H1-hESC	embryonic stem cell:	n/a	n/a
42	RAD21	chr15:73660645-73661422	H1-hESC	embryonic stem cell:	n/a	chr15:73660729-73660743
43	REST	chr15:73660354-73662087	H1-neurons	neurons:	n/a	chr15:73661985-73661995 chr15:73661347-73661357 chr15:73661296-73661306
44	RFX5	chr15:73661880-73662017	H1-hESC	embryonic stem cell:	n/a	n/a
45	RFX5	chr15:73662382-73662917	H1-hESC	embryonic stem cell:	n/a	n/a
46	SIN3A	chr15:73659134-73662077	H1-hESC	embryonic stem cell:	n/a	chr15:73660833-73660844
47	SIN3AK20	chr15:73660749-73661325	H1-hESC	embryonic stem cell:	n/a	n/a
48	TAF1	chr15:73660798-73661075	H1-hESC	embryonic stem cell:	n/a	n/a
49	TAF1	chr15:73661049-73661495	H1-neurons	neurons:	n/a	n/a
50	TAF1	chr15:73660706-73661201	H1-hESC	embryonic stem cell:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:73661340-73661390	AoSMC	blood vessel:	n/a
2	chr15:73662002-73662052	PrEC	prostate:	n/a
3	chr15:73659939-73659989	HCT-116	colon:	n/a
4	chr15:73660614-73660664	HCM	heart:	n/a
5	chr15:73661908-73661958	A549	lung:	n/a
6	chr15:73662002-73662052	AG04449	skin:	fetal
7	chr15:73661735-73661785	HMEC	breast:	n/a
8	chr15:73661735-73661785	GM12892	blood:	n/a
9	chr15:73661484-73661534	GM12892	blood:	n/a
10	chr15:73662258-73662308	HRE	kidney:	n/a
11	chr15:73661642-73661692	PrEC	prostate:	n/a
12	chr15:73661484-73661534	ovcar-3	ovarian:	n/a
13	chr15:73660614-73660664	HUVEC	blood vessel:	n/a
14	chr15:73661769-73661819	NHDF-neo	bronchial:	n/a
15	chr15:73661908-73661958	ProgFib	skin:	n/a
16	chr15:73659939-73659989	SK-N-SH_RA	brain:	n/a
17	chr15:73661769-73661819	HEEpiC	esophagus:	n/a
18	chr15:73661735-73661785	MCF10A-Er-Src	breast:	n/a
19	chr15:73661642-73661692	Jurkat	blood:	n/a
20	chr15:73661769-73661819	HCT-116	colon:	n/a
21	chr15:73659939-73659989	HCM	heart:	n/a
22	chr15:73661484-73661534	U87	brain:	n/a
23	chr15:73660614-73660664	ECC-1	luminal epithelium:	n/a
24	chr15:73659939-73659989	LNCaP	prostate:	n/a
25	chr15:73660614-73660664	CMK	blood:	n/a
26	chr15:73662258-73662308	A549	lung:	n/a
27	chr15:73661340-73661390	Jurkat	blood:	n/a
28	chr15:73662258-73662308	HRPEpiC	eye:	n/a
29	chr15:73661735-73661785	NT2-D1	testis:	n/a
30	chr15:73661340-73661390	Hela-S3	cervix:	n/a
31	chr15:73659939-73659989	RPTEC	kidney:	n/a
32	chr15:73661642-73661692	NB4	blood:	n/a
33	chr15:73661642-73661692	HUVEC	blood vessel:	n/a
34	chr15:73662258-73662308	Hela-S3	cervix:	n/a
35	chr15:73659861-73659911	SK-N-SH	brain:	n/a
36	chr15:73661652-73661702	AG09309	skin:	n/a
37	chr15:73659939-73659989	HEK293	kidney:	embryo
38	chr15:73660614-73660664	U87	brain:	n/a
39	chr15:73661652-73661702	AG04449	skin:	fetal
40	chr15:73661652-73661702	LNCaP	prostate:	n/a
41	chr15:73661908-73661958	SK-N-SH	brain:	n/a
42	chr15:73662258-73662308	AG09319	gingival:	n/a
43	chr15:73661652-73661702	AG10803	skin:	n/a
44	chr15:73661642-73661692	U87	brain:	n/a
45	chr15:73661484-73661534	LNCaP	prostate:	n/a
46	chr15:73661735-73661785	HCPEpiC	choroid plexus:	n/a
47	chr15:73659939-73659989	HepG2	liver:	n/a
48	chr15:73662002-73662052	NH-A	brain:	n/a
49	chr15:73661340-73661390	A549	lung:	n/a
50	chr15:73662258-73662308	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:73659851..73663146-chr15:73925069..73927598,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPTN-2	chr15:73660613-73661255	NONHSAT047146

No data

Variant related genes	Relation type
HCN4	TF binding region
HCN4	CpG island
ENSG00000156642	chromatin interactions

Extended variants
information (count: 113 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:113 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572691611	chr15:73659266-73659267	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs543343058	chr15:73659270-73659271	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs555205919	chr15:73659276-73659277	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs142157620	chr15:73659282-73659283	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs544339787	chr15:73659287-73659288	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs556930683	chr15:73659316-73659317	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs562416239	chr15:73659336-73659337	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs533030987	chr15:73659337-73659338	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs544719296	chr15:73659340-73659341	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs143109602	chr15:73659343-73659344	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs527582200	chr15:73659344-73659345	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs548823082	chr15:73659350-73659351	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs182680644	chr15:73659391-73659392	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs531371631	chr15:73659420-73659421	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561969591	chr15:73659429-73659430	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551604164	chr15:73659435-73659436	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376516331	chr15:73659443-73659444	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571372059	chr15:73659463-73659464	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148220500	chr15:73659482-73659483	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141188237	chr15:73659503-73659504	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150722554	chr15:73659507-73659508	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs137889000	chr15:73659612-73659613	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs566033956	chr15:73659643-73659644	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs145930956	chr15:73659720-73659721	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs114658768	chr15:73659737-73659738	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs555267414	chr15:73659749-73659750	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs200053779	chr15:73659777-73659778	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs201116986	chr15:73659795-73659796	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs188092263	chr15:73659798-73659799	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs573865102	chr15:73659814-73659815	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs368583153	chr15:73659829-73659830	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs191744064	chr15:73659869-73659870	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs370245193	chr15:73659870-73659871	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371771170	chr15:73659951-73659952	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545040345	chr15:73659979-73659980	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200186692	chr15:73660025-73660026	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs201375192	chr15:73660028-73660029	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375206856	chr15:73660051-73660052	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571671463	chr15:73660066-73660067	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs111892410	chr15:73660078-73660079	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369418464	chr15:73660084-73660085	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542532555	chr15:73660092-73660093	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560874115	chr15:73660154-73660155	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs531489450	chr15:73660167-73660168	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549753996	chr15:73660355-73660356	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143090627	chr15:73660505-73660506	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376849038	chr15:73660564-73660565	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201193660	chr15:73660576-73660577	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs547829940	chr15:73660645-73660646	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs566095713	chr15:73660741-73660742	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD

Chromatin state (count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73658400-73659400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
2	chr15:73658600-73659400	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
3	chr15:73658600-73659400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
4	chr15:73658600-73660000	Active TSS	Fetal Heart	heart
5	chr15:73658600-73661800	Active TSS	Right Atrium	heart
6	chr15:73658800-73659400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:73658800-73659600	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
8	chr15:73658800-73660000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
9	chr15:73658800-73660000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:73659000-73659400	Bivalent Enhancer	Fetal Brain Male	brain
11	chr15:73659000-73659600	Active TSS	H9 Cell Line	embryonic stem cell
12	chr15:73659000-73659600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
13	chr15:73659000-73659600	Enhancers	Pancreas	Pancrea
14	chr15:73659000-73660000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
15	chr15:73659000-73660000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr15:73659000-73660600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:73659200-73659400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr15:73659200-73659400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
19	chr15:73659200-73659400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
20	chr15:73659200-73659400	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
21	chr15:73659200-73659400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
22	chr15:73659200-73659600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr15:73659200-73659600	Active TSS	Right Ventricle	heart
24	chr15:73659200-73659800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr15:73659200-73659800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr15:73659200-73660000	Bivalent Enhancer	Placenta	Placenta
27	chr15:73659200-73660600	Bivalent Enhancer	Lung	lung
28	chr15:73659200-73661400	Active TSS	Left Ventricle	heart
29	chr15:73659200-73661600	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr15:73659200-73661800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
31	chr15:73659200-73662000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr15:73659400-73659600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
33	chr15:73659400-73659600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr15:73659400-73659600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr15:73659400-73659600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr15:73659400-73659800	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr15:73659400-73659800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr15:73659400-73659800	Bivalent Enhancer	Brain Anterior Caudate	brain
39	chr15:73659400-73659800	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
40	chr15:73659400-73659800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
41	chr15:73659400-73659800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
42	chr15:73659400-73660000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr15:73659400-73660000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
44	chr15:73659400-73660000	Bivalent Enhancer	Fetal Intestine Large	intestine
45	chr15:73659400-73660000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr15:73659400-73661200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
47	chr15:73659400-73661400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
48	chr15:73659400-73661800	Bivalent Enhancer	Spleen	Spleen
49	chr15:73659400-73662000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr15:73659400-73662000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

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