Variant report

Variant	esv3368275
Chromosome Location	chr15:34330085-34332358
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:428)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34330215-34330630	HepG2	liver:	n/a	n/a
2	BACH1	chr15:34330554-34331302	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr15:34331690-34332086	GM12878	blood:	n/a	n/a
4	BCLAF1	chr15:34331671-34332316	GM12878	blood:	n/a	n/a
5	BCLAF1	chr15:34330548-34331543	GM12878	blood:	n/a	chr15:34331510-34331519 chr15:34331505-34331518 chr15:34331281-34331294 chr15:34331311-34331320 chr15:34331500-34331513 chr15:34331250-34331263
6	BHLHE40	chr15:34330562-34331369	HepG2	liver:	n/a	n/a
7	BHLHE40	chr15:34331683-34332316	GM12878	blood:	n/a	n/a
8	BHLHE40	chr15:34330496-34330971	K562	blood:	n/a	n/a
9	BHLHE40	chr15:34330720-34331466	GM12878	blood:	n/a	n/a
10	BRCA1	chr15:34330077-34330584	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr15:34331653-34332077	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr15:34330358-34330700	K562	blood:	n/a	n/a
13	CBX3	chr15:34331138-34331442	K562	blood:	n/a	n/a
14	CCNT2	chr15:34330634-34331537	K562	blood:	n/a	n/a
15	CEBPB	chr15:34330202-34331257	Hela-S3	cervix:	n/a	n/a
16	CEBPD	chr15:34330716-34331126	HepG2	liver:	n/a	n/a
17	CHD1	chr15:34331164-34331484	GM12878	blood:	n/a	chr15:34331345-34331352
18	CHD2	chr15:34330413-34331500	Hela-S3	cervix:	n/a	chr15:34331345-34331352
19	CHD2	chr15:34331323-34331349	K562	blood:	n/a	n/a
20	CHD2	chr15:34330612-34330841	HepG2	liver:	n/a	n/a
21	CHD2	chr15:34330651-34330747	K562	blood:	n/a	n/a
22	CHD2	chr15:34331197-34331421	GM12878	blood:	n/a	chr15:34331345-34331352
23	CHD2	chr15:34330493-34330800	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr15:34330506-34331532	A549	lung:	n/a	n/a
25	CREB1	chr15:34331663-34332209	GM12878	blood:	n/a	n/a
26	CREB1	chr15:34331659-34332309	GM12878	blood:	n/a	n/a
27	CREB1	chr15:34330510-34331155	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr15:34330743-34331025	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr15:34330859-34330928	GM10266	blood:	n/a	n/a
30	CTCF	chr15:34331180-34331330	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr15:34331220-34331370	GM12866	blood:	n/a	n/a
32	CTCF	chr15:34330838-34330975	GM19239	blood:	n/a	n/a
33	CTCF	chr15:34330900-34331050	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr15:34330845-34330952	GM19238	blood:	n/a	n/a
35	CTCF	chr15:34330925-34330937	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr15:34330778-34330986	GM12892	blood:	n/a	n/a
37	CTCF	chr15:34330580-34330730	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr15:34330840-34330990	GM12871	blood:	n/a	n/a
39	CTCF	chr15:34330914-34330920	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr15:34330884-34330965	MCF-7	breast:	n/a	n/a
41	CTCF	chr15:34330880-34330883	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:34331139-34331508	K562	blood:	n/a	n/a
43	CTCF	chr15:34330903-34330921	A549	lung:	n/a	n/a
44	CTCF	chr15:34331200-34331350	GM12868	blood:	n/a	n/a
45	CTCF	chr15:34330640-34330790	HRE	kidney:	n/a	n/a
46	CTCF	chr15:34330869-34330977	GM12891	blood:	n/a	n/a
47	CTCF	chr15:34330862-34330884	GM19240	blood:	n/a	n/a
48	CTCF	chr15:34330750-34331055	GM12878	blood:	n/a	n/a
49	CTCF	chr15:34330848-34330963	NHEK	skin:	n/a	n/a
50	CTCF	chr15:34331200-34331350	AG04449	skin:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34331198-34331248	ovcar-3	ovarian:	n/a
2	chr15:34331198-34331248	ovcar-3	ovarian:	n/a
3	chr15:34330588-34330638	A549	lung:	n/a
4	chr15:34331198-34331248	HPAEpiC	pulmonary alveolar:	n/a
5	chr15:34331514-34331564	Jurkat	blood:	n/a
6	chr15:34330894-34330944	NH-A	brain:	n/a
7	chr15:34331198-34331248	Jurkat	blood:	n/a
8	chr15:34330588-34330638	RPTEC	kidney:	n/a
9	chr15:34331514-34331564	Hela-S3	cervix:	n/a
10	chr15:34331557-34331607	Caco-2	colon:	n/a
11	chr15:34330588-34330638	BJ	skin:	n/a
12	chr15:34331514-34331564	CMK	blood:	n/a
13	chr15:34331514-34331564	PFSK-1	brain:	n/a
14	chr15:34331198-34331248	MCF-7	breast:	n/a
15	chr15:34331557-34331607	HRCEpiC	kidney:	n/a
16	chr15:34331888-34331938	U87	brain:	n/a
17	chr15:34331888-34331938	NT2-D1	testis:	n/a
18	chr15:34331514-34331564	ProgFib	skin:	n/a
19	chr15:34331557-34331607	SK-N-SH	brain:	n/a
20	chr15:34331888-34331938	SK-N-SH_RA	brain:	n/a
21	chr15:34331514-34331564	HNPCEpiC	eye:	n/a
22	chr15:34331390-34331440	SK-N-SH	brain:	n/a
23	chr15:34331390-34331440	HRPEpiC	eye:	n/a
24	chr15:34330894-34330944	SK-N-SH	brain:	n/a
25	chr15:34330588-34330638	HNPCEpiC	eye:	n/a
26	chr15:34331198-34331248	SKMC	muscle:	n/a
27	chr15:34331198-34331248	MCF10A-Er-Src	breast:	n/a
28	chr15:34330894-34330944	ovcar-3	ovarian:	n/a
29	chr15:34331390-34331440	NT2-D1	testis:	n/a
30	chr15:34330588-34330638	HRE	kidney:	n/a
31	chr15:34331557-34331607	SAEC	small airway:	n/a
32	chr15:34331390-34331440	HRE	kidney:	n/a
33	chr15:34331390-34331440	HL-60	blood:	n/a
34	chr15:34331390-34331440	GM12878	blood:	n/a
35	chr15:34330588-34330638	AG04450	lung:	fetal
36	chr15:34331557-34331607	HepG2	liver:	n/a
37	chr15:34331514-34331564	PANC-1	pancreas:	n/a
38	chr15:34331198-34331248	A549	lung:	n/a
39	chr15:34331557-34331607	HCT-116	colon:	n/a
40	chr15:34331514-34331564	AG04450	lung:	fetal
41	chr15:34331390-34331440	PANC-1	pancreas:	n/a
42	chr15:34330894-34330944	GM12892	blood:	n/a
43	chr15:34331514-34331564	HL-60	blood:	n/a
44	chr15:34331514-34331564	IMR90	lung:	fetal
45	chr15:34331514-34331564	Hepatocyte	liver:	n/a
46	chr15:34331514-34331564	HEEpiC	esophagus:	n/a
47	chr15:34330894-34330944	LNCaP	prostate:	n/a
48	chr15:34331390-34331440	MCF-7	breast:	n/a
49	chr15:34331888-34331938	GM06990	blood:	n/a
50	chr15:34330588-34330638	HUVEC	blood vessel:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:34330538..34331100-chr16:778184..778756,2	HCT-116	colon:
2	chr15:34330950..34333091-chr15:34501411..34503652,2	K562	blood:
3	chr15:34330580..34331316-chrX:49028626..49029256,2	NB4	blood:
4	chr15:34330374..34330923-chr15:34659512..34660213,2	K562	blood:
5	chr15:34330580..34331391-chr19:10443789..10444410,2	NB4	blood:
6	chr12:54388393..54389358-chr15:34330438..34331617,3	Hela-S3	cervix:
7	chr1:45987162..45987999-chr15:34330632..34331222,2	NB4	blood:
8	chr15:34330893..34331669-chr9:132388498..132389170,2	Hela-S3	cervix:
9	chr15:34330614..34331132-chr22:21984221..21984750,2	NB4	blood:
10	chr12:49525016..49525540-chr15:34330682..34331291,2	HCT-116	colon:
11	chr15:34329770..34332450-chr15:34500868..34502911,3	K562	blood:
12	chr15:34327076..34328752-chr15:34329743..34331266,2	MCF-7	breast:
13	chr15:34320977..34323643-chr15:34328767..34331333,2	MCF-7	breast:
14	chr1:231003799..231004442-chr15:34330464..34331002,2	Hela-S3	cervix:
15	chr15:34330030..34332710-chr15:35259474..35262090,2	MCF-7	breast:

No data

Variant related genes	Relation type
AVEN	TF binding region
AVEN	CpG island
ENSG00000123416	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000103253	chromatin interactions
ENSG00000180806	chromatin interactions
ENSG00000148335	chromatin interactions
ENSG00000161847	chromatin interactions
ENSG00000161179	chromatin interactions
ENSG00000134152	chromatin interactions
ENSG00000021776	chromatin interactions
ENSG00000197757	chromatin interactions
ENSG00000119280	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561746385	chr15:34330102-34330103	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs2702275	chr15:34330162-34330163	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs145163520	chr15:34330229-34330230	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs375551030	chr15:34330333-34330334	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs559641219	chr15:34330357-34330358	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs532777730	chr15:34330359-34330360	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550990557	chr15:34330377-34330378	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs187888369	chr15:34330403-34330404	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs549641149	chr15:34330416-34330417	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536765600	chr15:34330446-34330447	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs547440707	chr15:34330464-34330465	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs549126183	chr15:34330472-34330473	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs567761302	chr15:34330481-34330482	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs535268021	chr15:34330491-34330492	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs112381581	chr15:34330494-34330495	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs147017879	chr15:34330588-34330589	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs539011010	chr15:34330618-34330619	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs557410126	chr15:34330670-34330671	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs370913068	chr15:34330683-34330684	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
20	rs114411704	chr15:34330747-34330748	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
21	rs111748206	chr15:34330786-34330787	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
22	rs145017745	chr15:34330811-34330812	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
23	rs71119920	chr15:34330819-34330820	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
24	rs72055078	chr15:34330829-34330830	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
25	rs555781217	chr15:34330850-34330851	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
26	rs561482649	chr15:34330858-34330859	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
27	rs573746809	chr15:34330931-34330932	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs541256726	chr15:34330942-34330943	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs192378891	chr15:34331000-34331001	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
30	rs533081558	chr15:34331002-34331003	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
31	rs550927187	chr15:34331107-34331108	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs562954080	chr15:34331111-34331112	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs530475689	chr15:34331113-34331114	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs2859666	chr15:34331124-34331125	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs548665164	chr15:34331215-34331216	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs567393546	chr15:34331265-34331266	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs112609265	chr15:34331290-34331291	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs562056195	chr15:34331333-34331334	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs571818226	chr15:34331402-34331403	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs539352964	chr15:34331408-34331409	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs538246427	chr15:34331409-34331410	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs565493110	chr15:34331472-34331473	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs185746002	chr15:34331501-34331502	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs569274779	chr15:34331529-34331530	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs536688466	chr15:34331532-34331533	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs11464486	chr15:34331580-34331581	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs398118727	chr15:34331581-34331582	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs79729332	chr15:34331582-34331583	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs188261893	chr15:34331601-34331602	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs554751508	chr15:34331609-34331610	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	6 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:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34326600-34330200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:34328400-34330400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:34329400-34331600	Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr15:34329600-34331600	Active TSS	GM12878-XiMat	blood
5	chr15:34329800-34330200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:34329800-34330200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr15:34329800-34330200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr15:34329800-34330200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
9	chr15:34329800-34330400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:34329800-34330400	Flanking Active TSS	A549	lung
11	chr15:34329800-34330400	Flanking Active TSS	Dnd41	blood
12	chr15:34329800-34330600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr15:34329800-34330800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr15:34329800-34331600	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr15:34329800-34331600	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr15:34330000-34330200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:34330000-34330200	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr15:34330000-34330200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr15:34330000-34330200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr15:34330000-34330200	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr15:34330000-34330200	Enhancers	Primary B cells from peripheral blood	blood
22	chr15:34330000-34330200	Active TSS	Primary hematopoietic stem cells	blood
23	chr15:34330000-34330200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:34330000-34330200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr15:34330000-34330200	Flanking Active TSS	Brain Anterior Caudate	brain
26	chr15:34330000-34330200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr15:34330000-34330200	Enhancers	Colon Smooth Muscle	Colon
28	chr15:34330000-34330200	Enhancers	Fetal Heart	heart
29	chr15:34330000-34330200	Flanking Active TSS	Fetal Lung	lung
30	chr15:34330000-34330200	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr15:34330000-34330200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr15:34330000-34330200	Enhancers	Stomach Mucosa	stomach
33	chr15:34330000-34330200	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr15:34330000-34330200	Flanking Active TSS	Hela-S3	cervix
35	chr15:34330000-34330200	Flanking Active TSS	HMEC	breast
36	chr15:34330000-34330200	Flanking Active TSS	HSMM	muscle
37	chr15:34330000-34330200	Active TSS	HSMMtube	muscle
38	chr15:34330000-34330200	Active TSS	K562	blood
39	chr15:34330000-34330200	Flanking Active TSS	NHDF-Ad	bronchial
40	chr15:34330000-34330200	Flanking Active TSS	NHLF	lung
41	chr15:34330000-34330400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
42	chr15:34330000-34330400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr15:34330000-34330400	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr15:34330000-34330400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr15:34330000-34330400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr15:34330000-34330400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr15:34330000-34330400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
48	chr15:34330000-34330400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
49	chr15:34330000-34330400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr15:34330000-34330400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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