Variant report

Variant	nsv903986
Chromosome Location	chr15:34394273-34421951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:969)
CpG islands
(count:488)
Chromatin interactive
region (count:41)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:969 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34393681-34394773	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:34403426-34403439	K562	blood:	n/a	n/a
3	ARID3A	chr15:34402362-34402600	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:34402309-34402652	K562	blood:	n/a	n/a
5	ARID3A	chr15:34394020-34394474	K562	blood:	n/a	n/a
6	ATF1	chr15:34393917-34394573	K562	blood:	n/a	n/a
7	ATF2	chr15:34393917-34394425	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:34393860-34394355	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:34393901-34394585	GM12878	blood:	n/a	n/a
10	ATF2	chr15:34414899-34415466	GM12878	blood:	n/a	n/a
11	ATF2	chr15:34393805-34394669	GM12878	blood:	n/a	n/a
12	ATF3	chr15:34393858-34394377	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr15:34393937-34394330	K562	blood:	n/a	n/a
14	ATF3	chr15:34393859-34394435	GM12878	blood:	n/a	n/a
15	ATF3	chr15:34393736-34394572	A549	lung:	n/a	n/a
16	ATF3	chr15:34393643-34394339	K562	blood:	n/a	n/a
17	ATF3	chr15:34393843-34394517	A549	lung:	n/a	n/a
18	ATF3	chr15:34393914-34394305	HepG2	liver:	n/a	n/a
19	ATF3	chr15:34393835-34394379	HepG2	liver:	n/a	n/a
20	ATF3	chr15:34393971-34394379	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:34394099-34394585	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr15:34394195-34394625	K562	blood:	n/a	n/a
23	BATF	chr15:34415082-34415462	GM12878	blood:	n/a	n/a
24	BATF	chr15:34394026-34394483	GM12878	blood:	n/a	chr15:34394119-34394132
25	BATF	chr15:34415056-34415524	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:34415028-34415505	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:34415027-34415412	GM12878	blood:	n/a	n/a
28	BCL3	chr15:34393590-34394781	A549	lung:	n/a	chr15:34394101-34394110 chr15:34394101-34394114
29	BCL3	chr15:34393643-34394523	A549	lung:	n/a	chr15:34394101-34394110 chr15:34394101-34394114
30	BCLAF1	chr15:34393725-34394641	GM12878	blood:	n/a	chr15:34394101-34394110 chr15:34394101-34394114
31	BCLAF1	chr15:34393788-34394594	GM12878	blood:	n/a	chr15:34394101-34394110 chr15:34394101-34394114
32	BHLHE40	chr15:34414921-34415443	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:34393872-34394631	HepG2	liver:	n/a	n/a
34	BHLHE40	chr15:34393874-34394657	K562	blood:	n/a	n/a
35	BHLHE40	chr15:34393955-34394662	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:34394879-34395135	K562	blood:	n/a	n/a
37	BRCA1	chr15:34393900-34394577	GM12878	blood:	n/a	n/a
38	BRCA1	chr15:34402312-34402533	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr15:34393832-34394561	HepG2	liver:	n/a	n/a
40	BRCA1	chr15:34393988-34394414	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr15:34393889-34394472	Hela-S3	cervix:	n/a	n/a
42	CBX3	chr15:34394023-34394630	K562	blood:	n/a	n/a
43	CBX3	chr15:34393803-34394564	K562	blood:	n/a	n/a
44	CCNT2	chr15:34393806-34394375	K562	blood:	n/a	n/a
45	CEBPB	chr15:34399558-34399890	Hela-S3	cervix:	n/a	chr15:34399708-34399719
46	CEBPB	chr15:34414179-34414229	HepG2	liver:	n/a	chr15:34414191-34414202
47	CEBPB	chr15:34393927-34394330	K562	blood:	n/a	n/a
48	CEBPB	chr15:34393798-34394667	GM12878	blood:	n/a	n/a
49	CEBPB	chr15:34393904-34394447	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr15:34393971-34394385	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34396328-34396378	BE2_C	brain:	n/a
2	chr15:34396328-34396378	NT2-D1	testis:	n/a
3	chr15:34396248-34396298	GM12891	blood:	n/a
4	chr15:34394376-34394426	AG10803	skin:	n/a
5	chr15:34396328-34396378	SKMC	muscle:	n/a
6	chr15:34394263-34394313	HCM	heart:	n/a
7	chr15:34395546-34395596	NT2-D1	testis:	n/a
8	chr15:34396328-34396378	AG09309	skin:	n/a
9	chr15:34396328-34396378	NHBE	bronchial:	n/a
10	chr15:34396328-34396378	A549	lung:	n/a
11	chr15:34395540-34395590	AG10803	skin:	n/a
12	chr15:34396248-34396298	CMK	blood:	n/a
13	chr15:34394376-34394426	NT2-D1	testis:	n/a
14	chr15:34394376-34394426	LNCaP	prostate:	n/a
15	chr15:34396328-34396378	GM19239	blood:	n/a
16	chr15:34415586-34415636	U87	brain:	n/a
17	chr15:34415586-34415636	NH-A	brain:	n/a
18	chr15:34394376-34394426	ECC-1	luminal epithelium:	n/a
19	chr15:34395546-34395596	HEK293	kidney:	embryo
20	chr15:34394263-34394313	ovcar-3	ovarian:	n/a
21	chr15:34394263-34394313	HL-60	blood:	n/a
22	chr15:34395540-34395590	HEEpiC	esophagus:	n/a
23	chr15:34394376-34394426	HRE	kidney:	n/a
24	chr15:34394260-34394310	GM19239	blood:	n/a
25	chr15:34394376-34394426	U87	brain:	n/a
26	chr15:34395540-34395590	Hepatocyte	liver:	n/a
27	chr15:34395540-34395590	GM12891	blood:	n/a
28	chr15:34396328-34396378	HRE	kidney:	n/a
29	chr15:34396248-34396298	ovcar-3	ovarian:	n/a
30	chr15:34394376-34394426	HEEpiC	esophagus:	n/a
31	chr15:34395540-34395590	ovcar-3	ovarian:	n/a
32	chr15:34395540-34395590	SKMC	muscle:	n/a
33	chr15:34396328-34396378	AG04449	skin:	fetal
34	chr15:34395540-34395590	GM19239	blood:	n/a
35	chr15:34394260-34394310	GM12878	blood:	n/a
36	chr15:34396328-34396378	HepG2	liver:	n/a
37	chr15:34396328-34396378	IMR90	lung:	fetal
38	chr15:34395546-34395596	HAEpiC	amniotic membrane:	n/a
39	chr15:34396328-34396378	Jurkat	blood:	n/a
40	chr15:34395540-34395590	LNCaP	prostate:	n/a
41	chr15:34395540-34395590	HRPEpiC	eye:	n/a
42	chr15:34394260-34394310	IMR90	lung:	fetal
43	chr15:34415586-34415636	PFSK-1	brain:	n/a
44	chr15:34396328-34396378	PrEC	prostate:	n/a
45	chr15:34395546-34395596	HL-60	blood:	n/a
46	chr15:34394260-34394310	MCF-7	breast:	n/a
47	chr15:34394260-34394310	BJ	skin:	n/a
48	chr15:34396328-34396378	BJ	skin:	n/a
49	chr15:34396328-34396378	LNCaP	prostate:	n/a
50	chr15:34395540-34395590	MCF10A-Er-Src	breast:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:34331236..34333239-chr15:34415576..34418277,2	MCF-7	breast:
2	chr15:34417003..34419819-chr15:34499362..34502166,2	K562	blood:
3	chr15:34393973..34395738-chr15:34396163..34397953,2	K562	blood:
4	chr15:34410925..34412547-chr15:34416896..34419566,2	K562	blood:
5	chr15:34395145..34398026-chr15:34628783..34630423,2	K562	blood:
6	chr15:34402323..34402946-chr15:34504244..34504792,2	MCF-7	breast:
7	chr15:34419776..34421652-chr15:34425219..34427967,2	MCF-7	breast:
8	chr15:34393239..34395470-chr15:34515986..34518807,4	MCF-7	breast:
9	chr15:34401986..34402589-chr15:34502207..34502829,2	MCF-7	breast:
10	chr15:34391885..34395742-chr15:34500701..34502399,4	K562	blood:
11	chr15:34402914..34405409-chr15:34502231..34505059,2	K562	blood:
12	chr15:34411334..34412247-chr15:34501831..34502833,4	MCF-7	breast:
13	chr15:34397749..34399755-chr15:34409612..34411614,2	K562	blood:
14	chr15:34402115..34404646-chr15:34407237..34411184,3	K562	blood:
15	chr15:34402131..34404554-chr15:34408275..34409911,2	K562	blood:
16	chr15:34394473..34397367-chr15:34405065..34407483,2	K562	blood:
17	chr15:34393898..34395784-chr15:34415043..34417474,3	MCF-7	breast:
18	chr15:34391225..34395745-chr15:34498845..34504196,8	K562	blood:
19	chr15:34392784..34394847-chr15:34629052..34631553,2	K562	blood:
20	chr1:45265565..45266510-chr15:34394011..34394570,2	Hela-S3	cervix:
21	chr14:35342985..35344751-chr15:34393746..34395266,2	MCF-7	breast:
22	chr15:34392855..34396101-chr15:34515904..34518783,5	MCF-7	breast:
23	chr15:34401848..34402956-chr15:34501932..34502951,5	K562	blood:
24	chr15:34420038..34421927-chr15:34425295..34427888,2	K562	blood:
25	chr15:34391770..34396248-chr15:34515474..34518631,5	K562	blood:
26	chr15:34401088..34402962-chr15:34501811..34503818,2	MCF-7	breast:
27	chr15:34410925..34412547-chr15:34416896..34419566,2	K562	blood:
28	chr15:34391943..34394373-chr15:34406757..34408689,2	K562	blood:
29	chr15:34402115..34404646-chr15:34407237..34411184,3	K562	blood:
30	chr15:34393027..34394938-chr15:34659377..34661190,2	K562	blood:
31	chr15:34393027..34397233-chr15:34658612..34660877,5	K562	blood:
32	chr15:34401890..34403731-chr15:34532079..34534352,2	MCF-7	breast:
33	chr15:34397749..34399755-chr15:34409612..34411614,2	K562	blood:
34	chr15:34405220..34406883-chr15:34500622..34502410,2	MCF-7	breast:
35	chr15:34394445..34396841-chr15:34644524..34647284,2	K562	blood:
36	chr15:34394246..34396074-chr15:34398306..34400604,2	MCF-7	breast:
37	chr15:34402458..34403052-chr15:34501962..34502479,2	MCF-7	breast:
38	chr15:34402131..34404554-chr15:34408275..34409911,2	K562	blood:
39	chr15:34394473..34397367-chr15:34405065..34407483,2	K562	blood:
40	chr15:34402010..34402956-chr15:34659467..34660260,3	K562	blood:
41	chr15:34402294..34404744-chr15:34506028..34509076,3	MCF-7	breast:

No data

Variant related genes	Relation type
PGBD4	TF binding region
EMC7	TF binding region
PGBD4	CpG island
EMC7	CpG island
ENSG00000173846	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000134153	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000182405	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000134152	chromatin interactions
ENSG00000258738	chromatin interactions

Extended variants
information (count: 1116 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1116 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1436923	chr15:34394273-34394274	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs151117787	chr15:34394302-34394303	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs531888223	chr15:34394315-34394316	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs550731167	chr15:34394324-34394325	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs568993151	chr15:34394329-34394330	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs142602469	chr15:34394347-34394348	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs548208037	chr15:34394368-34394369	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs566084234	chr15:34394384-34394385	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs537178230	chr15:34394437-34394438	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs556625484	chr15:34394445-34394446	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs533552055	chr15:34394503-34394504	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs552239177	chr15:34394530-34394531	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs551794462	chr15:34394570-34394571	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs570208292	chr15:34394577-34394578	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs570578546	chr15:34394602-34394603	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs575462033	chr15:34394625-34394626	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs538083763	chr15:34394634-34394635	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs369100101	chr15:34394704-34394705	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs371746226	chr15:34394710-34394711	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs373391573	chr15:34394736-34394737	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs369128610	chr15:34394741-34394742	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs191002477	chr15:34394800-34394801	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs144743527	chr15:34394840-34394841	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs77459405	chr15:34394871-34394872	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs148121524	chr15:34394876-34394877	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs368069858	chr15:34394877-34394878	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs146817012	chr15:34394878-34394879	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs141885404	chr15:34394882-34394883	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs139272250	chr15:34394908-34394909	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs73374372	chr15:34394926-34394927	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs374986308	chr15:34394945-34394946	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs201334800	chr15:34394971-34394972	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs141734203	chr15:34395000-34395001	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs370035921	chr15:34395006-34395007	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs576596254	chr15:34395007-34395008	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs35595072	chr15:34395013-34395014	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs552902642	chr15:34395018-34395019	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs140024325	chr15:34395034-34395035	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs543566180	chr15:34395108-34395109	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs373518770	chr15:34395125-34395126	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs375166420	chr15:34395194-34395195	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs201137112	chr15:34395198-34395199	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs199891832	chr15:34395231-34395232	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs202141977	chr15:34395256-34395257	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs75481258	chr15:34395279-34395280	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs560002445	chr15:34395283-34395284	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs201890653	chr15:34395349-34395350	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs547379354	chr15:34395366-34395367	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs527624224	chr15:34395372-34395373	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs202024701	chr15:34395373-34395374	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:452 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34391800-34394800	Active TSS	GM12878-XiMat	blood
2	chr15:34392200-34394600	Active TSS	Rectal Smooth Muscle	rectum
3	chr15:34392400-34394800	Active TSS	K562	blood
4	chr15:34392400-34394800	Active TSS	NHLF	lung
5	chr15:34392400-34395400	Active TSS	Psoas Muscle	Psoas
6	chr15:34392600-34394600	Active TSS	Stomach Smooth Muscle	stomach
7	chr15:34392600-34395000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:34392600-34395000	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr15:34392600-34395000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr15:34392600-34395200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr15:34392800-34394600	Active TSS	Brain Inferior Temporal Lobe	brain
12	chr15:34392800-34394600	Active TSS	Fetal Kidney	kidney
13	chr15:34392800-34394800	Active TSS	Fetal Intestine Small	intestine
14	chr15:34392800-34394800	Active TSS	Fetal Muscle Leg	muscle
15	chr15:34392800-34394800	Active TSS	Right Atrium	heart
16	chr15:34392800-34394800	Active TSS	HSMMtube	muscle
17	chr15:34392800-34395200	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr15:34392800-34395200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr15:34392800-34395400	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr15:34392800-34395600	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr15:34393000-34394600	Active TSS	Esophagus	oesophagus
22	chr15:34393000-34394600	Active TSS	Lung	lung
23	chr15:34393000-34394600	Active TSS	Sigmoid Colon	Sigmoid Colon
24	chr15:34393000-34394800	Active TSS	H1 Cell Line	embryonic stem cell
25	chr15:34393000-34394800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr15:34393000-34394800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:34393000-34394800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr15:34393000-34394800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr15:34393000-34394800	Active TSS	Fetal Stomach	stomach
30	chr15:34393000-34394800	Active TSS	Fetal Thymus	thymus
31	chr15:34393000-34394800	Active TSS	Left Ventricle	heart
32	chr15:34393000-34394800	Active TSS	NHDF-Ad	bronchial
33	chr15:34393000-34394800	Active TSS	NHEK	skin
34	chr15:34393000-34395000	Active TSS	H9 Cell Line	embryonic stem cell
35	chr15:34393000-34395000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr15:34393000-34395000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr15:34393000-34395000	Active TSS	Aorta	Aorta
38	chr15:34393000-34395000	Active TSS	Fetal Muscle Trunk	muscle
39	chr15:34393000-34395000	Active TSS	Ovary	ovary
40	chr15:34393000-34395000	Active TSS	Right Ventricle	heart
41	chr15:34393000-34395000	Active TSS	Stomach Mucosa	stomach
42	chr15:34393200-34394400	Active TSS	Hela-S3	cervix
43	chr15:34393200-34394600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr15:34393200-34394600	Active TSS	iPS-18 Cell Line	embryonic stem cell
45	chr15:34393200-34394600	Active TSS	Muscle Satellite Cultured Cells	--
46	chr15:34393200-34394600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
47	chr15:34393200-34394600	Active TSS	Fetal Heart	heart
48	chr15:34393200-34394600	Active TSS	Small Intestine	intestine
49	chr15:34393200-34394800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr15:34393200-34394800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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