Variant report

Variant	nsv825955
Chromosome Location	chr11:66035970-66036506
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	ATF2	chr11:66035493-66036088	GM12878	blood:	n/a	n/a
2	ATF2	chr11:66035569-66036047	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr11:66035105-66036118	GM12878	blood:	n/a	n/a
4	ATF2	chr11:66035490-66035983	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr11:66034682-66036155	A549	lung:	n/a	chr11:66036135-66036148 chr11:66036137-66036150 chr11:66036140-66036149 chr11:66035930-66035939 chr11:66035443-66035456 chr11:66036071-66036080 chr11:66035677-66035686 chr11:66036137-66036146
6	BCL3	chr11:66035066-66036187	A549	lung:	n/a	chr11:66036135-66036148 chr11:66036137-66036150 chr11:66036140-66036149 chr11:66035930-66035939 chr11:66035443-66035456 chr11:66036071-66036080 chr11:66035677-66035686 chr11:66036137-66036146
7	BCLAF1	chr11:66036316-66036662	GM12878	blood:	n/a	n/a
8	BCLAF1	chr11:66035188-66036035	GM12878	blood:	n/a	chr11:66035930-66035939 chr11:66035443-66035456 chr11:66035677-66035686
9	BHLHE40	chr11:66034705-66036494	GM12878	blood:	n/a	chr11:66036134-66036150
10	BHLHE40	chr11:66036399-66036593	K562	blood:	n/a	n/a
11	BHLHE40	chr11:66034706-66036038	K562	blood:	n/a	n/a
12	BRCA1	chr11:66035795-66036091	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr11:66034703-66035982	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr11:66035503-66036010	K562	blood:	n/a	n/a
15	CCNT2	chr11:66034905-66036238	K562	blood:	n/a	n/a
16	CEBPB	chr11:66035779-66036025	Hela-S3	cervix:	n/a	n/a
17	CEBPD	chr11:66035662-66036555	HepG2	liver:	n/a	n/a
18	CHD1	chr11:66036270-66037446	GM12878	blood:	n/a	chr11:66036317-66036327
19	CHD1	chr11:66033899-66037453	IMR90	lung:	n/a	chr11:66036317-66036327
20	CHD2	chr11:66035674-66036503	HepG2	liver:	n/a	chr11:66036317-66036327
21	CHD2	chr11:66035674-66036508	Hela-S3	cervix:	n/a	chr11:66036317-66036327
22	CHD2	chr11:66035620-66036428	H1-hESC	embryonic stem cell:	n/a	chr11:66036317-66036327
23	CHD2	chr11:66034842-66036666	K562	blood:	n/a	chr11:66036317-66036327
24	CHD2	chr11:66034824-66036604	GM12878	blood:	n/a	chr11:66036317-66036327
25	CREB1	chr11:66035708-66036134	ECC-1	luminal epithelium:	n/a	n/a
26	CREB1	chr11:66034773-66036351	GM12878	blood:	n/a	n/a
27	CREB1	chr11:66035458-66036280	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr11:66035709-66036030	A549	lung:	n/a	n/a
29	CREB1	chr11:66035683-66036256	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr11:66035517-66036103	ECC-1	luminal epithelium:	n/a	n/a
31	CREB1	chr11:66034989-66036349	A549	lung:	n/a	n/a
32	CTCF	chr11:66035998-66036002	Spleen_OC	spleen:	n/a	n/a
33	CTCF	chr11:66036012-66036068	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr11:66036480-66036630	HepG2	liver:	n/a	n/a
35	CTCF	chr11:66036500-66036650	AG04450	lung:	n/a	n/a
36	CTCF	chr11:66036360-66036510	GM12871	blood:	n/a	chr11:66036390-66036399
37	E2F1	chr11:66035766-66036137	Hela-S3	cervix:	n/a	chr11:66035956-66035965 chr11:66036056-66036065 chr11:66035935-66035944 chr11:66036073-66036082 chr11:66036043-66036052
38	E2F4	chr11:66035507-66036019	GM12878	blood:	n/a	chr11:66035956-66035965 chr11:66035935-66035944
39	E2F4	chr11:66035254-66036288	K562	blood:	n/a	chr11:66036139-66036149 chr11:66035956-66035965 chr11:66036056-66036065 chr11:66036136-66036146 chr11:66036174-66036183 chr11:66035935-66035944 chr11:66036073-66036082 chr11:66036043-66036052
40	E2F4	chr11:66035584-66036160	MCF10A-Er-Src	breast:	n/a	chr11:66036139-66036149 chr11:66035956-66035965 chr11:66036056-66036065 chr11:66036136-66036146 chr11:66035935-66035944 chr11:66036073-66036082 chr11:66036043-66036052
41	E2F6	chr11:66035819-66035993	K562	blood:	n/a	chr11:66035956-66035965 chr11:66035935-66035944
42	EBF1	chr11:66034894-66036089	GM12878	blood:	n/a	chr11:66035235-66035246
43	EBF1	chr11:66035638-66035974	GM12878	blood:	n/a	n/a
44	EGR1	chr11:66035772-66036307	K562	blood:	n/a	chr11:66036043-66036052 chr11:66035886-66035910 chr11:66036261-66036274 chr11:66035993-66036017 chr11:66035930-66035943 chr11:66035927-66035937 chr11:66036294-66036304 chr11:66035922-66035935
45	EGR1	chr11:66035695-66036093	K562	blood:	n/a	chr11:66036043-66036052 chr11:66035886-66035910 chr11:66035993-66036017 chr11:66035930-66035943 chr11:66035927-66035937 chr11:66035922-66035935
46	EGR1	chr11:66035786-66036002	GM12878	blood:	n/a	chr11:66035886-66035910 chr11:66035930-66035943 chr11:66035927-66035937 chr11:66035922-66035935
47	EGR1	chr11:66035649-66036336	MCF-7	breast:	n/a	chr11:66036043-66036052 chr11:66035886-66035910 chr11:66036261-66036274 chr11:66035993-66036017 chr11:66035930-66035943 chr11:66035927-66035937 chr11:66036294-66036304 chr11:66035922-66035935
48	ELF1	chr11:66035687-66037247	MCF-7	breast:	n/a	chr11:66036302-66036313 chr11:66036137-66036149 chr11:66036302-66036313 chr11:66035933-66035945 chr11:66036141-66036150 chr11:66035932-66035941 chr11:66036138-66036147
49	ELF1	chr11:66035628-66037193	MCF-7	breast:	n/a	chr11:66036302-66036313 chr11:66036137-66036149 chr11:66036302-66036313 chr11:66035933-66035945 chr11:66036141-66036150 chr11:66035932-66035941 chr11:66036138-66036147
50	ELF1	chr11:66035704-66036496	HepG2	liver:	n/a	chr11:66036302-66036313 chr11:66036137-66036149 chr11:66036302-66036313 chr11:66035933-66035945 chr11:66036141-66036150 chr11:66035932-66035941 chr11:66036138-66036147

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:66036125-66036175	AG10803	skin:	n/a
2	chr11:66035940-66035990	Caco-2	colon:	n/a
3	chr11:66036125-66036175	AG10803	skin:	n/a
4	chr11:66035940-66035990	Caco-2	colon:	n/a
5	chr11:66036125-66036175	GM19239	blood:	n/a
6	chr11:66036020-66036070	NB4	blood:	n/a
7	chr11:66035934-66035984	SK-N-SH	brain:	n/a
8	chr11:66036017-66036067	RPTEC	kidney:	n/a
9	chr11:66036005-66036055	NHBE	bronchial:	n/a
10	chr11:66036115-66036165	AoSMC	blood vessel:	n/a
11	chr11:66036125-66036175	PANC-1	pancreas:	n/a
12	chr11:66036038-66036088	AG09319	gingival:	n/a
13	chr11:66036005-66036055	BE2_C	brain:	n/a
14	chr11:66036005-66036055	HEK293	kidney:	embryo
15	chr11:66035942-66035992	Hela-S3	cervix:	n/a
16	chr11:66035951-66036001	A549	lung:	n/a
17	chr11:66035986-66036036	GM12878	blood:	n/a
18	chr11:66036020-66036070	AG04449	skin:	fetal
19	chr11:66035942-66035992	BE2_C	brain:	n/a
20	chr11:66035951-66036001	AG10803	skin:	n/a
21	chr11:66036125-66036175	HL-60	blood:	n/a
22	chr11:66035942-66035992	NHBE	bronchial:	n/a
23	chr11:66035940-66035990	Hepatocyte	liver:	n/a
24	chr11:66036138-66036188	AG04449	skin:	fetal
25	chr11:66035940-66035990	A549	lung:	n/a
26	chr11:66036115-66036165	H1-hESC	embryonic stem cell:	embryo
27	chr11:66035951-66036001	NH-A	brain:	n/a
28	chr11:66035942-66035992	NH-A	brain:	n/a
29	chr11:66036020-66036070	Jurkat	blood:	n/a
30	chr11:66036020-66036070	RPTEC	kidney:	n/a
31	chr11:66036038-66036088	SAEC	small airway:	n/a
32	chr11:66036038-66036088	NH-A	brain:	n/a
33	chr11:66036015-66036065	HAEpiC	amniotic membrane:	n/a
34	chr11:66035986-66036036	HCF	heart:	n/a
35	chr11:66036115-66036165	NT2-D1	testis:	n/a
36	chr11:66036125-66036175	H1-hESC	embryonic stem cell:	embryo
37	chr11:66035951-66036001	AG04449	skin:	fetal
38	chr11:66036038-66036088	HepG2	liver:	n/a
39	chr11:66036125-66036175	MCF-7	breast:	n/a
40	chr11:66035932-66035982	GM06990	blood:	n/a
41	chr11:66035951-66036001	AoSMC	blood vessel:	n/a
42	chr11:66036038-66036088	Caco-2	colon:	n/a
43	chr11:66035986-66036036	SK-N-MC	brain:	n/a
44	chr11:66036015-66036065	HL-60	blood:	n/a
45	chr11:66035934-66035984	PrEC	prostate:	n/a
46	chr11:66035940-66035990	SK-N-SH	brain:	n/a
47	chr11:66036138-66036188	HMEC	breast:	n/a
48	chr11:66036125-66036175	SK-N-SH_RA	brain:	n/a
49	chr11:66035986-66036036	AG04450	lung:	fetal
50	chr11:66035942-66035992	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:66036063..66037921-chr11:66134364..66136433,2	K562	blood:
2	chr11:65625132..65628506-chr11:66035169..66036764,3	K562	blood:
3	chr11:65728121..65730647-chr11:66035766..66038196,2	MCF-7	breast:
4	chr11:66035942..66036494-chr15:41576128..41576906,2	Hela-S3	cervix:
5	chr11:66035942..66036615-chr19:8578822..8579342,2	HCT-116	colon:
6	chr11:65657107..65659864-chr11:66036057..66038289,3	MCF-7	breast:
7	chr11:66035212..66038142-chr11:66136666..66139462,2	MCF-7	breast:
8	chr11:66035609..66037495-chr11:66113505..66115336,2	MCF-7	breast:
9	chr11:65624298..65626384-chr11:66036037..66037653,2	MCF-7	breast:
10	chr11:66025383..66026303-chr11:66034980..66036455,5	K562	blood:
11	chr11:65666389..65668880-chr11:66033377..66036542,3	K562	blood:
12	chr11:66034858..66038328-chr11:66053749..66060447,9	MCF-7	breast:
13	chr11:65998798..66000841-chr11:66035751..66037263,2	K562	blood:
14	chr11:65655875..65658695-chr11:66035091..66037770,2	MCF-7	breast:
15	chr1:37979819..37980754-chr11:66035320..66036263,2	Hela-S3	cervix:
16	chr11:66035321..66036213-chr5:176852911..176853534,2	HCT-116	colon:
17	chr1:65885913..65886852-chr11:66036167..66036667,2	Hela-S3	cervix:
18	chr11:66035872..66036377-chr16:31008172..31008955,2	Hela-S3	cervix:
19	chr11:66034904..66037277-chr17:57914562..57916871,2	MCF-7	breast:
20	chr11:66036265..66039186-chr11:66074799..66077052,2	MCF-7	breast:
21	chr11:65624882..65627968-chr11:66034504..66038316,6	K562	blood:

Variant related genes	Relation type
ENSG00000254762	TF binding region
ENSG00000254855	TF binding region
RAB1B	TF binding region
ENSG00000254762	CpG island
ENSG00000254855	CpG island
RAB1B	CpG island
ENSG00000062716	chromatin interactions
ENSG00000172500	chromatin interactions
ENSG00000116678	chromatin interactions
ENSG00000163875	chromatin interactions
ENSG00000247556	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000175467	chromatin interactions
ENSG00000175115	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000213625	chromatin interactions
ENSG00000198055	chromatin interactions
ENSG00000175602	chromatin interactions
ENSG00000099365	chromatin interactions
ENSG00000174669	chromatin interactions
ENSG00000175592	chromatin interactions
ENSG00000174996	chromatin interactions
ENSG00000174684	chromatin interactions
ENSG00000179292	chromatin interactions
ENSG00000133250	chromatin interactions

Extended variants
information (count: 27 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3814739	chr11:66035979-66035980	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531867664	chr11:66035983-66035984	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
3	rs551465085	chr11:66035990-66035991	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
4	rs567878444	chr11:66036028-66036029	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
5	rs11227440	chr11:66036041-66036042	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
6	rs56372222	chr11:66036047-66036048	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
7	rs547725725	chr11:66036077-66036078	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
8	rs112419770	chr11:66036078-66036079	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
9	rs567424548	chr11:66036090-66036091	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
10	rs536470200	chr11:66036134-66036135	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
11	rs199656742	chr11:66036141-66036142	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
12	rs71461617	chr11:66036181-66036182	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
13	rs371004043	chr11:66036197-66036198	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
14	rs569633935	chr11:66036252-66036253	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
15	rs150627444	chr11:66036293-66036294	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
16	rs386374030	chr11:66036300-66036301	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
17	rs55687530	chr11:66036302-66036303	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
18	rs538752721	chr11:66036342-66036343	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
19	rs558263478	chr11:66036369-66036370	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
20	rs571747644	chr11:66036371-66036372	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
21	rs540484978	chr11:66036372-66036373	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
22	rs554046970	chr11:66036373-66036374	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
23	rs571025829	chr11:66036382-66036383	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
24	rs542837009	chr11:66036403-66036404	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
25	rs187704608	chr11:66036435-66036436	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
26	rs538551100	chr11:66036456-66036457	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
27	rs531709786	chr11:66036488-66036489	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66032800-66036000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:66034200-66036000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr11:66034400-66036000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr11:66034400-66036000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:66034400-66036800	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr11:66034400-66037000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr11:66034400-66037000	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr11:66034400-66037000	Active TSS	Fetal Kidney	kidney
9	chr11:66034400-66037200	Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr11:66034600-66036000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr11:66034600-66036000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr11:66034600-66036600	Active TSS	Placenta Amnion	Placenta Amnion
13	chr11:66034600-66036800	Active TSS	iPS-18 Cell Line	embryonic stem cell
14	chr11:66034600-66037000	Active TSS	H9 Cell Line	embryonic stem cell
15	chr11:66034600-66037000	Active TSS	Brain Anterior Caudate	brain
16	chr11:66034600-66037000	Active TSS	Colon Smooth Muscle	Colon
17	chr11:66034600-66037000	Active TSS	Fetal Lung	lung
18	chr11:66034600-66037000	Active TSS	Left Ventricle	heart
19	chr11:66034600-66037200	Active TSS	H1 Cell Line	embryonic stem cell
20	chr11:66034600-66037200	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr11:66034600-66037200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr11:66034600-66037200	Active TSS	Aorta	Aorta
23	chr11:66034600-66037200	Active TSS	Ovary	ovary
24	chr11:66034600-66037400	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr11:66034800-66036000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
26	chr11:66034800-66036000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:66034800-66036000	Flanking Active TSS	Fetal Thymus	thymus
28	chr11:66034800-66036600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:66034800-66036600	Active TSS	Cortex derived primary cultured neurospheres	brain
30	chr11:66034800-66036600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr11:66034800-66036600	Active TSS	Brain Germinal Matrix	brain
32	chr11:66034800-66036600	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr11:66034800-66036600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
34	chr11:66034800-66036600	Active TSS	Fetal Brain Male	brain
35	chr11:66034800-66036600	Active TSS	Fetal Intestine Small	intestine
36	chr11:66034800-66036800	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr11:66034800-66036800	Active TSS	Primary T killer memory cells from peripheral blood	blood
38	chr11:66034800-66036800	Active TSS	Brain Angular Gyrus	brain
39	chr11:66034800-66036800	Active TSS	Brain Hippocampus Middle	brain
40	chr11:66034800-66036800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr11:66034800-66036800	Active TSS	Brain Substantia Nigra	brain
42	chr11:66034800-66036800	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr11:66034800-66036800	Active TSS	Fetal Brain Female	brain
44	chr11:66034800-66036800	Active TSS	Fetal Stomach	stomach
45	chr11:66034800-66036800	Active TSS	Rectal Smooth Muscle	rectum
46	chr11:66034800-66036800	Active TSS	Spleen	Spleen
47	chr11:66034800-66037000	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr11:66034800-66037000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:66034800-66037000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:66034800-66037000	Active TSS	Gastric	stomach

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