Variant report

Variant	esv3344912
Chromosome Location	chr15:43028085-43030633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43030048-43030327	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:43029205-43029320	HepG2	liver:	n/a	n/a
3	ATF3	chr15:43029026-43029443	K562	blood:	n/a	n/a
4	BACH1	chr15:43029146-43029218	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr15:43029194-43029684	K562	blood:	n/a	chr15:43029327-43029343
6	BHLHE40	chr15:43029125-43029621	GM12878	blood:	n/a	chr15:43029327-43029343
7	BRCA1	chr15:43029093-43029475	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr15:43029963-43030363	K562	blood:	n/a	n/a
9	CBX3	chr15:43029043-43029634	K562	blood:	n/a	n/a
10	CCNT2	chr15:43028482-43029698	K562	blood:	n/a	n/a
11	CEBPB	chr15:43030134-43030327	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr15:43029236-43029574	Hela-S3	cervix:	n/a	n/a
13	CEBPD	chr15:43029131-43029486	HepG2	liver:	n/a	n/a
14	CHD1	chr15:43028787-43029166	GM12878	blood:	n/a	n/a
15	CHD2	chr15:43029512-43029626	HepG2	liver:	n/a	n/a
16	CHD2	chr15:43028738-43028847	HepG2	liver:	n/a	n/a
17	CHD2	chr15:43029865-43030006	K562	blood:	n/a	n/a
18	CHD2	chr15:43028887-43029640	Hela-S3	cervix:	n/a	n/a
19	CHD2	chr15:43029402-43029581	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr15:43029116-43029266	K562	blood:	n/a	n/a
21	CHD2	chr15:43029073-43029293	HepG2	liver:	n/a	n/a
22	CHD2	chr15:43029167-43029173	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr15:43029474-43029674	GM12878	blood:	n/a	n/a
24	CREB1	chr15:43029120-43029386	A549	lung:	n/a	n/a
25	CREB1	chr15:43028993-43029648	K562	blood:	n/a	n/a
26	CTCF	chr15:43029140-43029290	GM12872	blood:	n/a	chr15:43029185-43029195
27	CTCF	chr15:43029100-43029250	GM12871	blood:	n/a	chr15:43029185-43029195
28	CTCF	chr15:43029180-43029330	SAEC	small airway:	n/a	chr15:43029185-43029195
29	CTCF	chr15:43029160-43029310	AG04449	skin:	n/a	chr15:43029185-43029195
30	CTCF	chr15:43030150-43030332	K562	blood:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
31	CTCF	chr15:43030029-43030446	MCF-7	breast:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
32	CTCF	chr15:43030089-43030400	A549	lung:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
33	CTCF	chr15:43030180-43030330	HPAF	blood vessel:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
34	CTCF	chr15:43029192-43029239	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr15:43029264-43029273	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr15:43030147-43030352	HepG2	liver:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
37	CTCF	chr15:43029180-43029330	GM12866	blood:	n/a	chr15:43029185-43029195
38	CTCF	chr15:43030140-43030290	HVMF	connective:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
39	CTCF	chr15:43029198-43029227	K562	blood:	n/a	n/a
40	CTCF	chr15:43029934-43030386	HCT-116	colon:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
41	CTCF	chr15:43029236-43029286	GM13977	blood:	n/a	n/a
42	CTCF	chr15:43030047-43030484	MCF-7	breast:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
43	CTCF	chr15:43030180-43030330	BJ	skin:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
44	CTCF	chr15:43030160-43030310	HEK293	kidney:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
45	CTCF	chr15:43030220-43030370	HCT-116	colon:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
46	CTCF	chr15:43030160-43030310	HPAF	blood vessel:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
47	CTCF	chr15:43030146-43030335	MCF-7	breast:	n/a	chr15:43030245-43030258 chr15:43030242-43030260
48	CTCF	chr15:43029182-43029275	MCF-7	breast:	n/a	chr15:43029185-43029195
49	CTCF	chr15:43029120-43029270	HBMEC	blood vessel:	n/a	chr15:43029185-43029195
50	CTCF	chr15:43030160-43030310	HCFaa	heart:	n/a	chr15:43030245-43030258 chr15:43030242-43030260

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43029438-43029488	Caco-2	colon:	n/a
2	chr15:43028463-43028513	SKMC	muscle:	n/a
3	chr15:43028916-43028966	NT2-D1	testis:	n/a
4	chr15:43029558-43029608	HUVEC	blood vessel:	n/a
5	chr15:43029558-43029608	HepG2	liver:	n/a
6	chr15:43029799-43029849	HCT-116	colon:	n/a
7	chr15:43028463-43028513	PFSK-1	brain:	n/a
8	chr15:43029438-43029488	NHBE	bronchial:	n/a
9	chr15:43028932-43028982	Jurkat	blood:	n/a
10	chr15:43029438-43029488	HIPEpiC	eye:	n/a
11	chr15:43029432-43029482	SK-N-MC	brain:	n/a
12	chr15:43029558-43029608	SKMC	muscle:	n/a
13	chr15:43029242-43029292	HCPEpiC	choroid plexus:	n/a
14	chr15:43029242-43029292	AG04449	skin:	fetal
15	chr15:43029799-43029849	GM06990	blood:	n/a
16	chr15:43029438-43029488	ovcar-3	ovarian:	n/a
17	chr15:43029242-43029292	HIPEpiC	eye:	n/a
18	chr15:43028932-43028982	HCPEpiC	choroid plexus:	n/a
19	chr15:43029242-43029292	BE2_C	brain:	n/a
20	chr15:43028463-43028513	GM12891	blood:	n/a
21	chr15:43029799-43029849	MCF-7	breast:	n/a
22	chr15:43028916-43028966	HCT-116	colon:	n/a
23	chr15:43029799-43029849	T-47D	breast:	n/a
24	chr15:43029432-43029482	CMK	blood:	n/a
25	chr15:43029799-43029849	RPTEC	kidney:	n/a
26	chr15:43029432-43029482	AG04450	lung:	fetal
27	chr15:43029242-43029292	MCF-7	breast:	n/a
28	chr15:43028916-43028966	HMEC	breast:	n/a
29	chr15:43028932-43028982	ovcar-3	ovarian:	n/a
30	chr15:43029558-43029608	AG09319	gingival:	n/a
31	chr15:43029242-43029292	HUVEC	blood vessel:	n/a
32	chr15:43029558-43029608	HEEpiC	esophagus:	n/a
33	chr15:43029643-43029693	ECC-1	luminal epithelium:	n/a
34	chr15:43029242-43029292	HepG2	liver:	n/a
35	chr15:43029799-43029849	U87	brain:	n/a
36	chr15:43028463-43028513	HCPEpiC	choroid plexus:	n/a
37	chr15:43029202-43029252	HMEC	breast:	n/a
38	chr15:43029242-43029292	AG09319	gingival:	n/a
39	chr15:43028932-43028982	HL-60	blood:	n/a
40	chr15:43029242-43029292	NB4	blood:	n/a
41	chr15:43029432-43029482	GM12892	blood:	n/a
42	chr15:43029202-43029252	HRCEpiC	kidney:	n/a
43	chr15:43028916-43028966	HCM	heart:	n/a
44	chr15:43028932-43028982	U87	brain:	n/a
45	chr15:43029799-43029849	SAEC	small airway:	n/a
46	chr15:43029558-43029608	AoSMC	blood vessel:	n/a
47	chr15:43029432-43029482	K562	blood:	n/a
48	chr15:43029438-43029488	IMR90	lung:	fetal
49	chr15:43028463-43028513	HNPCEpiC	eye:	n/a
50	chr15:43029799-43029849	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:43029097..43029683-chr8:22102019..22102704,2	HCT-116	colon:
2	chr15:43014319..43018768-chr15:43027782..43030873,5	MCF-7	breast:
3	chr15:43019448..43022159-chr15:43025632..43028520,2	MCF-7	breast:
4	chr15:43028764..43029357-chr7:100183650..100184158,2	Hela-S3	cervix:
5	chr15:43029256..43031403-chr15:43210732..43214178,4	K562	blood:

Variant related genes	Relation type
ENSG00000246283	TF binding region
CDAN1	TF binding region
ENSG00000246283	CpG island
CDAN1	CpG island
ENSG00000077454	chromatin interactions
ENSG00000106336	chromatin interactions
ENSG00000128881	chromatin interactions
ENSG00000140326	chromatin interactions
ENSG00000168495	chromatin interactions
ENSG00000208037	chromatin interactions

Extended variants
information (count: 107 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:107 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199787046	chr15:43028085-43028086	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs184207000	chr15:43028089-43028090	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372653695	chr15:43028099-43028100	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs139936073	chr15:43028115-43028116	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs571317942	chr15:43028141-43028142	Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs143391538	chr15:43028207-43028208	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs112317805	chr15:43028222-43028223	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs200994232	chr15:43028241-43028242	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs374111927	chr15:43028244-43028245	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146716516	chr15:43028252-43028253	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs530521066	chr15:43028278-43028279	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs375923006	chr15:43028287-43028288	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370228678	chr15:43028294-43028295	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs560630349	chr15:43028338-43028339	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs529704255	chr15:43028340-43028341	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs188826309	chr15:43028369-43028370	Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546310338	chr15:43028412-43028413	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs566611704	chr15:43028429-43028430	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538462509	chr15:43028431-43028432	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs552437769	chr15:43028433-43028434	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs569103717	chr15:43028459-43028460	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs377303707	chr15:43028472-43028473	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs200071287	chr15:43028510-43028511	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs12594325	chr15:43028511-43028512	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs370085664	chr15:43028515-43028516	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs370757859	chr15:43028521-43028522	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373153188	chr15:43028542-43028543	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs376335465	chr15:43028571-43028572	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs369344224	chr15:43028575-43028576	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574099736	chr15:43028579-43028580	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs372759056	chr15:43028586-43028587	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs7167392	chr15:43028592-43028593	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs556698310	chr15:43028610-43028611	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs73410959	chr15:43028626-43028627	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs372488868	chr15:43028631-43028632	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs376536296	chr15:43028643-43028644	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs12441516	chr15:43028683-43028684	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs4265781	chr15:43028749-43028750	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575562332	chr15:43028760-43028761	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs543791953	chr15:43028813-43028814	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs180857061	chr15:43028832-43028833	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs529640896	chr15:43028851-43028852	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs186189866	chr15:43028912-43028913	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs80338694	chr15:43028913-43028914	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs560030704	chr15:43028955-43028956	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs532331365	chr15:43028958-43028959	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs552114001	chr15:43028962-43028963	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs374298277	chr15:43029027-43029028	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs538104452	chr15:43029065-43029066	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs75649060	chr15:43029066-43029067	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 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	20164920	CNVD
Hodgkin''s lymphoma	18641027	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
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43018400-43028200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr15:43023600-43028400	Weak transcription	Small Intestine	intestine
3	chr15:43024800-43028200	Weak transcription	NH-A	brain
4	chr15:43026400-43028200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr15:43026800-43028200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr15:43026800-43028200	Genic enhancers	Thymus	Thymus
7	chr15:43026800-43028400	Genic enhancers	Primary T cells fromperipheralblood	blood
8	chr15:43027200-43028200	Genic enhancers	Fetal Lung	lung
9	chr15:43027200-43028200	Transcr. at gene 5' and 3'	Dnd41	blood
10	chr15:43027200-43028400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr15:43027400-43028200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:43027400-43028200	Weak transcription	Fetal Kidney	kidney
13	chr15:43027600-43028200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr15:43027600-43028200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr15:43027600-43028200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr15:43027600-43028200	Enhancers	Fetal Heart	heart
17	chr15:43027600-43028200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr15:43027600-43028400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr15:43027600-43028400	Enhancers	Spleen	Spleen
20	chr15:43027600-43028600	Flanking Active TSS	Colon Smooth Muscle	Colon
21	chr15:43027800-43028200	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr15:43027800-43028200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:43027800-43028200	Enhancers	Brain Hippocampus Middle	brain
24	chr15:43027800-43028200	Enhancers	Esophagus	oesophagus
25	chr15:43027800-43028200	Enhancers	Fetal Brain Male	brain
26	chr15:43027800-43028200	Genic enhancers	Fetal Thymus	thymus
27	chr15:43027800-43028200	Enhancers	Ovary	ovary
28	chr15:43027800-43028200	Enhancers	Right Ventricle	heart
29	chr15:43027800-43028400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr15:43027800-43028400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr15:43027800-43028600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr15:43027800-43028600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr15:43027800-43028600	Flanking Active TSS	Hela-S3	cervix
34	chr15:43027800-43028800	Enhancers	Stomach Mucosa	stomach
35	chr15:43028000-43028200	Active TSS	ES-I3 Cell Line	embryonic stem cell
36	chr15:43028000-43028200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:43028000-43028200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:43028000-43028200	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr15:43028000-43028200	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr15:43028000-43028200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
41	chr15:43028000-43028200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr15:43028000-43028200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr15:43028000-43028200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr15:43028000-43028200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr15:43028000-43028200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr15:43028000-43028200	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr15:43028000-43028200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr15:43028000-43028200	Enhancers	Primary T cells from cord blood	blood
49	chr15:43028000-43028200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr15:43028000-43028200	Transcr. at gene 5' and 3'	Cortex derived primary cultured neurospheres	brain

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