Variant report

Variant	esv1808787
Chromosome Location	chr15:73660269-73664741
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:672)
Chromatin interactive
region (count:1)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:73661673-73662017	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr15:73660382-73660487	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	CREB1	chr15:73660758-73661270	A549	lung:	n/a	n/a
6	CTBP2	chr15:73660453-73662080	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr15:73661660-73661810	HEK293	kidney:	n/a	n/a
8	E2F6	chr15:73661598-73662138	H1-hESC	embryonic stem cell:	n/a	n/a
9	E2F6	chr15:73661021-73662142	H1-hESC	embryonic stem cell:	n/a	chr15:73661348-73661358 chr15:73661368-73661377
10	EGR1	chr15:73660750-73661091	H1-hESC	embryonic stem cell:	n/a	chr15:73660850-73660860
11	GABPA	chr15:73660218-73660719	H1-hESC	embryonic stem cell:	n/a	n/a
12	HA-E2F1	chr15:73660599-73661316	MCF-7	breast:	n/a	n/a
13	JUN	chr15:73662674-73662725	HepG2	liver:	n/a	chr15:73662684-73662693 chr15:73662683-73662696
14	JUND	chr15:73660801-73660981	H1-hESC	embryonic stem cell:	n/a	n/a
15	JUND	chr15:73661110-73661363	H1-hESC	embryonic stem cell:	n/a	n/a
16	MAX	chr15:73661092-73662035	H1-hESC	embryonic stem cell:	n/a	chr15:73661277-73661286 chr15:73661186-73661195
17	MAX	chr15:73661643-73662133	H1-hESC	embryonic stem cell:	n/a	n/a
18	MXI1	chr15:73661812-73662012	H1-hESC	embryonic stem cell:	n/a	n/a
19	MXI1	chr15:73660358-73660443	H1-hESC	embryonic stem cell:	n/a	n/a
20	MXI1	chr15:73660738-73661344	H1-hESC	embryonic stem cell:	n/a	chr15:73661277-73661292
21	POLR2A	chr15:73660982-73661251	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr15:73661556-73661928	H1-neurons	neurons:	n/a	n/a
23	POLR2A	chr15:73662634-73662788	GM12878	blood:	n/a	n/a
24	POLR2A	chr15:73661446-73661976	H1-neurons	neurons:	n/a	n/a
25	POLR2A	chr15:73660880-73661126	MCF-7	breast:	n/a	n/a
26	POLR2A	chr15:73660755-73661299	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr15:73660679-73661446	H1-neurons	neurons:	n/a	n/a
28	POLR2A	chr15:73660870-73660876	MCF-7	breast:	n/a	n/a
29	POLR2A	chr15:73660730-73661394	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr15:73661014-73661278	HCT-116	colon:	n/a	n/a
31	POLR2A	chr15:73661065-73661066	Gliobla	brain:	n/a	n/a
32	POLR2A	chr15:73660132-73660634	H1-neurons	neurons:	n/a	n/a
33	POLR2A	chr15:73660360-73661393	H1-neurons	neurons:	n/a	n/a
34	POLR2A	chr15:73660536-73661506	H1-hESC	embryonic stem cell:	n/a	n/a
35	RAD21	chr15:73660645-73661422	H1-hESC	embryonic stem cell:	n/a	chr15:73660729-73660743
36	REST	chr15:73660354-73662087	H1-neurons	neurons:	n/a	chr15:73661985-73661995 chr15:73661347-73661357 chr15:73661296-73661306
37	RFX5	chr15:73661880-73662017	H1-hESC	embryonic stem cell:	n/a	n/a
38	RFX5	chr15:73662382-73662917	H1-hESC	embryonic stem cell:	n/a	n/a
39	SIN3A	chr15:73659134-73662077	H1-hESC	embryonic stem cell:	n/a	chr15:73660833-73660844
40	SIN3AK20	chr15:73660749-73661325	H1-hESC	embryonic stem cell:	n/a	n/a
41	TAF1	chr15:73661049-73661495	H1-neurons	neurons:	n/a	n/a
42	TAF1	chr15:73660798-73661075	H1-hESC	embryonic stem cell:	n/a	n/a
43	TAF1	chr15:73660706-73661201	H1-hESC	embryonic stem cell:	n/a	n/a
44	TBP	chr15:73660773-73661311	H1-hESC	embryonic stem cell:	n/a	n/a
45	TEAD4	chr15:73664126-73664474	H1-hESC	embryonic stem cell:	n/a	n/a
46	TEAD4	chr15:73664139-73664483	H1-hESC	embryonic stem cell:	n/a	n/a
47	YY1	chr15:73660704-73661321	H1-hESC	embryonic stem cell:	n/a	chr15:73661298-73661312 chr15:73660969-73660978 chr15:73660723-73660737 chr15:73660967-73660978
48	YY1	chr15:73660810-73661007	HCT-116	colon:	n/a	chr15:73660969-73660978 chr15:73660967-73660978
49	ZBTB7A	chr15:73661158-73661632	ECC-1	luminal epithelium:	n/a	chr15:73661360-73661367
50	ZNF263	chr15:73659877-73661052	HEK293-T-REx	kidney:	n/a	chr15:73660820-73660829

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:73661735-73661785	HCPEpiC	choroid plexus:	n/a
2	chr15:73661735-73661785	HCPEpiC	choroid plexus:	n/a
3	chr15:73661908-73661958	GM12878	blood:	n/a
4	chr15:73661340-73661390	K562	blood:	n/a
5	chr15:73662002-73662052	HRPEpiC	eye:	n/a
6	chr15:73662002-73662052	SKMC	muscle:	n/a
7	chr15:73661735-73661785	BJ	skin:	n/a
8	chr15:73660614-73660664	GM12892	blood:	n/a
9	chr15:73664318-73664368	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:73661652-73661702	Hela-S3	cervix:	n/a
11	chr15:73661769-73661819	GM12892	blood:	n/a
12	chr15:73661652-73661702	PrEC	prostate:	n/a
13	chr15:73664318-73664368	BJ	skin:	n/a
14	chr15:73661735-73661785	NB4	blood:	n/a
15	chr15:73661652-73661702	AG04450	lung:	fetal
16	chr15:73661642-73661692	Caco-2	colon:	n/a
17	chr15:73661642-73661692	SAEC	small airway:	n/a
18	chr15:73661484-73661534	Hela-S3	cervix:	n/a
19	chr15:73661769-73661819	AG09309	skin:	n/a
20	chr15:73660614-73660664	HRPEpiC	eye:	n/a
21	chr15:73661642-73661692	HEK293	kidney:	embryo
22	chr15:73661908-73661958	GM06990	blood:	n/a
23	chr15:73661735-73661785	HCF	heart:	n/a
24	chr15:73661484-73661534	A549	lung:	n/a
25	chr15:73661769-73661819	HIPEpiC	eye:	n/a
26	chr15:73662258-73662308	HCT-116	colon:	n/a
27	chr15:73662258-73662308	SK-N-SH_RA	brain:	n/a
28	chr15:73661908-73661958	Caco-2	colon:	n/a
29	chr15:73660614-73660664	GM19239	blood:	n/a
30	chr15:73661484-73661534	AG10803	skin:	n/a
31	chr15:73661484-73661534	HIPEpiC	eye:	n/a
32	chr15:73661340-73661390	HL-60	blood:	n/a
33	chr15:73664318-73664368	AG09319	gingival:	n/a
34	chr15:73662002-73662052	AG09309	skin:	n/a
35	chr15:73662002-73662052	Hela-S3	cervix:	n/a
36	chr15:73661908-73661958	BJ	skin:	n/a
37	chr15:73661735-73661785	HUVEC	blood vessel:	n/a
38	chr15:73661908-73661958	Jurkat	blood:	n/a
39	chr15:73661484-73661534	NHBE	bronchial:	n/a
40	chr15:73661340-73661390	NT2-D1	testis:	n/a
41	chr15:73661652-73661702	BJ	skin:	n/a
42	chr15:73661642-73661692	NH-A	brain:	n/a
43	chr15:73661735-73661785	HNPCEpiC	eye:	n/a
44	chr15:73662002-73662052	HMEC	breast:	n/a
45	chr15:73661484-73661534	HCT-116	colon:	n/a
46	chr15:73661642-73661692	HCM	heart:	n/a
47	chr15:73660614-73660664	BJ	skin:	n/a
48	chr15:73661642-73661692	Hepatocyte	liver:	n/a
49	chr15:73661340-73661390	SKMC	muscle:	n/a
50	chr15:73661908-73661958	AG09309	skin:	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: 138 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:138 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	rs536621293	chr15:73660781-73660782	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
8	rs548581131	chr15:73660800-73660801	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs577671006	chr15:73660879-73660880	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs183675842	chr15:73661018-73661019	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs537745479	chr15:73661047-73661048	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs146150604	chr15:73661109-73661110	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs577325559	chr15:73661158-73661159	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs188896349	chr15:73661179-73661180	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs538368084	chr15:73661193-73661194	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs140161530	chr15:73661196-73661197	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs536533926	chr15:73661297-73661298	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs571784371	chr15:73661303-73661304	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs556778812	chr15:73661350-73661351	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577297264	chr15:73661502-73661503	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs192441254	chr15:73661543-73661544	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576307973	chr15:73661546-73661547	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs543657107	chr15:73661646-73661647	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs564942952	chr15:73661668-73661669	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs532299569	chr15:73661680-73661681	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs7172796	chr15:73661687-73661688	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs559915826	chr15:73661700-73661701	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530208347	chr15:73661784-73661785	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs548648330	chr15:73661818-73661819	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs570018767	chr15:73661837-73661838	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376486089	chr15:73661884-73661885	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs531119987	chr15:73661908-73661909	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs552800030	chr15:73661926-73661927	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs545557018	chr15:73661953-73661954	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs558387352	chr15:73661977-73661978	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs370785808	chr15:73661986-73661987	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs553133459	chr15:73661987-73661988	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565479936	chr15:73662051-73662052	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs184586130	chr15:73662097-73662098	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs61253286	chr15:73662119-73662120	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554149374	chr15:73662151-73662152	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35540703	chr15:73662218-73662219	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs3028614	chr15:73662223-73662224	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs575954627	chr15:73662227-73662228	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543368289	chr15:73662240-73662241	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558788212	chr15:73662250-73662251	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577041847	chr15:73662278-73662279	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs374508929	chr15:73662358-73662359	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541263704	chr15:73662380-73662381	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs559583298	chr15:73662455-73662456	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 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:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73658600-73661800	Active TSS	Right Atrium	heart
2	chr15:73659000-73660600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:73659200-73660600	Bivalent Enhancer	Lung	lung
4	chr15:73659200-73661400	Active TSS	Left Ventricle	heart
5	chr15:73659200-73661600	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr15:73659200-73661800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
7	chr15:73659200-73662000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr15:73659400-73661200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
9	chr15:73659400-73661400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
10	chr15:73659400-73661800	Bivalent Enhancer	Spleen	Spleen
11	chr15:73659400-73662000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr15:73659400-73662000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
13	chr15:73659400-73662200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
14	chr15:73659400-73662200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
15	chr15:73659600-73661400	Flanking Active TSS	Pancreas	Pancrea
16	chr15:73659600-73661800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr15:73659600-73662200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
18	chr15:73659600-73662200	Bivalent/Poised TSS	Fetal Brain Female	brain
19	chr15:73659800-73660400	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
20	chr15:73659800-73661000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
21	chr15:73659800-73661200	Enhancers	Liver	Liver
22	chr15:73659800-73661400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr15:73659800-73661600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr15:73659800-73661800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr15:73659800-73662000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr15:73660000-73660400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr15:73660000-73660400	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr15:73660000-73660400	Bivalent Enhancer	Ovary	ovary
29	chr15:73660000-73660400	Bivalent/Poised TSS	Psoas Muscle	Psoas
30	chr15:73660000-73660400	Flanking Active TSS	Right Ventricle	heart
31	chr15:73660000-73661200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
32	chr15:73660000-73661200	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr15:73660000-73661400	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr15:73660000-73661400	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr15:73660000-73661400	Active TSS	iPS-15b Cell Line	embryonic stem cell
36	chr15:73660000-73661400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
37	chr15:73660000-73661400	Weak transcription	Fetal Heart	heart
38	chr15:73660000-73661800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
39	chr15:73660000-73661800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr15:73660000-73661800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr15:73660000-73662200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
42	chr15:73660000-73662200	Active TSS	H9 Cell Line	embryonic stem cell
43	chr15:73660200-73660400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
44	chr15:73660200-73660400	Flanking Active TSS	Primary hematopoietic stem cells	blood
45	chr15:73660200-73660400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
46	chr15:73660200-73660400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr15:73660200-73660400	Bivalent/Poised TSS	Adipose Nuclei	Adipose
48	chr15:73660200-73660400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
49	chr15:73660200-73660400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
50	chr15:73660200-73660400	Flanking Active TSS	Gastric	stomach

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