Variant report

Variant	nsv975369
Chromosome Location	chr11:102219075-102221776
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	BRCA1	chr11:102219071-102219225	Hela-S3	cervix:	n/a	n/a
2	CHD1	chr11:102216324-102220503	IMR90	lung:	n/a	n/a
3	CHD1	chr11:102219803-102219805	GM12878	blood:	n/a	n/a
4	CHD1	chr11:102216702-102219105	GM12878	blood:	n/a	n/a
5	CTCF	chr11:102217289-102219193	SK-N-SH	brain:	n/a	n/a
6	CTCF	chr11:102218940-102219090	HMEC	breast:	n/a	n/a
7	CTCF	chr11:102221380-102221530	HMEC	breast:	n/a	n/a
8	CTCF	chr11:102221260-102221410	NHDF-neo	bronchial:	n/a	n/a
9	CTCF	chr11:102221400-102221550	NHDF-neo	bronchial:	n/a	n/a
10	CTCF	chr11:102221280-102221430	HPAF	blood vessel:	n/a	n/a
11	CTCF	chr11:102218960-102219110	NHDF-neo	bronchial:	n/a	n/a
12	CTCF	chr11:102221340-102221490	AG09319	gingival:	n/a	n/a
13	CTCF	chr11:102221440-102221590	HAc	cerebellar:	n/a	n/a
14	CTCF	chr11:102221415-102221485	GM12878	blood:	n/a	n/a
15	CTCF	chr11:102221340-102221490	GM06990	blood:	n/a	n/a
16	CTCF	chr11:102221360-102221510	HMEC	breast:	n/a	n/a
17	CTCF	chr11:102218940-102219090	RPTEC	kidney:	n/a	n/a
18	E2F4	chr11:102218783-102219154	MCF10A-Er-Src	breast:	n/a	n/a
19	EBF1	chr11:102218476-102219092	GM12878	blood:	n/a	n/a
20	FOXA1	chr11:102219554-102220164	HepG2	liver:	n/a	chr11:102219789-102219804 chr11:102219978-102219990
21	FOXA1	chr11:102219750-102219996	HepG2	liver:	n/a	chr11:102219789-102219804 chr11:102219978-102219990
22	FOXA1	chr11:102219564-102220204	HepG2	liver:	n/a	chr11:102219789-102219804 chr11:102219978-102219990
23	FOXA1	chr11:102219695-102220046	HepG2	liver:	n/a	chr11:102219789-102219804 chr11:102219978-102219990
24	FOXA2	chr11:102219722-102220099	HepG2	liver:	n/a	chr11:102219978-102219990
25	FOXA2	chr11:102219450-102220415	HepG2	liver:	n/a	chr11:102219978-102219990
26	GATA1	chr11:102217395-102219234	PBDE	blood:	n/a	chr11:102218253-102218264 chr11:102218686-102218699
27	HCFC1	chr11:102217253-102219500	Hela-S3	cervix:	n/a	n/a
28	HEY1	chr11:102218797-102219084	HepG2	liver:	n/a	n/a
29	HEY1	chr11:102218702-102219135	HepG2	liver:	n/a	n/a
30	IRF1	chr11:102221441-102221475	K562	blood:	n/a	n/a
31	IRF1	chr11:102217582-102219142	K562	blood:	n/a	chr11:102218776-102218787 chr11:102218774-102218788 chr11:102217864-102217884 chr11:102218776-102218789 chr11:102218587-102218601 chr11:102217860-102217877 chr11:102218776-102218789 chr11:102218771-102218788 chr11:102218173-102218182
32	JUN	chr11:102216330-102219183	K562	blood:	n/a	chr11:102217937-102217946 chr11:102218106-102218117 chr11:102218105-102218113 chr11:102217933-102217946
33	JUND	chr11:102216544-102219211	SK-N-SH	brain:	n/a	chr11:102217937-102217946 chr11:102218106-102218117 chr11:102218105-102218113
34	MAX	chr11:102217306-102219139	NB4	blood:	n/a	chr11:102217767-102217778 chr11:102218136-102218145
35	MXI1	chr11:102217086-102219200	IMR90	lung:	n/a	n/a
36	MXI1	chr11:102218535-102219120	Hela-S3	cervix:	n/a	n/a
37	MYC	chr11:102218805-102219105	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr11:102217300-102219113	K562	blood:	n/a	chr11:102217767-102217778 chr11:102218136-102218145
39	MYC	chr11:102217274-102219091	NB4	blood:	n/a	chr11:102217767-102217778 chr11:102218136-102218145
40	MYC	chr11:102218573-102219120	MCF10A-Er-Src	breast:	n/a	n/a
41	NFYA	chr11:102218895-102219131	Hela-S3	cervix:	n/a	n/a
42	NFYB	chr11:102218793-102219146	GM12878	blood:	n/a	n/a
43	NFYB	chr11:102218807-102219118	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr11:102220794-102221726	HepG2	liver:	n/a	n/a
45	POLR2A	chr11:102220950-102221409	HepG2	liver:	n/a	n/a
46	POLR2A	chr11:102221238-102221388	K562	blood:	n/a	n/a
47	POLR2A	chr11:102218797-102219176	SK-N-SH	brain:	n/a	n/a
48	POLR2A	chr11:102217172-102219089	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr11:102220961-102221008	HepG2	liver:	n/a	n/a
50	POLR2A	chr11:102216571-102219131	GM18505	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:102221100-102221150	ProgFib	skin:	n/a
2	chr11:102221100-102221150	AG09319	gingival:	n/a
3	chr11:102221100-102221150	HMEC	breast:	n/a
4	chr11:102221100-102221150	NH-A	brain:	n/a
5	chr11:102221100-102221150	AG04450	lung:	fetal
6	chr11:102221100-102221150	PANC-1	pancreas:	n/a
7	chr11:102221100-102221150	NHDF-neo	bronchial:	n/a
8	chr11:102221100-102221150	HCT-116	colon:	n/a
9	chr11:102221100-102221150	SK-N-MC	brain:	n/a
10	chr11:102221100-102221150	PFSK-1	brain:	n/a
11	chr11:102221100-102221150	U87	brain:	n/a
12	chr11:102221100-102221150	MCF-7	breast:	n/a
13	chr11:102221100-102221150	SKMC	muscle:	n/a
14	chr11:102221100-102221150	PrEC	prostate:	n/a
15	chr11:102221100-102221150	K562	blood:	n/a
16	chr11:102221100-102221150	GM12891	blood:	n/a
17	chr11:102221100-102221150	LNCaP	prostate:	n/a
18	chr11:102221100-102221150	AG04449	skin:	fetal
19	chr11:102221100-102221150	GM19239	blood:	n/a
20	chr11:102221100-102221150	NHBE	bronchial:	n/a
21	chr11:102221100-102221150	IMR90	lung:	fetal
22	chr11:102221100-102221150	ovcar-3	ovarian:	n/a
23	chr11:102221100-102221150	Hela-S3	cervix:	n/a
24	chr11:102221100-102221150	HIPEpiC	eye:	n/a
25	chr11:102221100-102221150	SK-N-SH	brain:	n/a
26	chr11:102221100-102221150	H1-hESC	embryonic stem cell:	embryo
27	chr11:102221100-102221150	Jurkat	blood:	n/a
28	chr11:102221100-102221150	BJ	skin:	n/a
29	chr11:102221100-102221150	HUVEC	blood vessel:	n/a
30	chr11:102221100-102221150	HEK293	kidney:	embryo
31	chr11:102221100-102221150	MCF10A-Er-Src	breast:	n/a
32	chr11:102221100-102221150	HRPEpiC	eye:	n/a
33	chr11:102221100-102221150	ECC-1	luminal epithelium:	n/a
34	chr11:102221100-102221150	HEEpiC	esophagus:	n/a
35	chr11:102221100-102221150	HRE	kidney:	n/a
36	chr11:102221100-102221150	HCF	heart:	n/a
37	chr11:102221100-102221150	SK-N-SH_RA	brain:	n/a
38	chr11:102221100-102221150	AoSMC	blood vessel:	n/a
39	chr11:102221100-102221150	SAEC	small airway:	n/a
40	chr11:102221100-102221150	HAEpiC	amniotic membrane:	n/a
41	chr11:102221100-102221150	AG09309	skin:	n/a
42	chr11:102221100-102221150	GM12892	blood:	n/a
43	chr11:102221100-102221150	NT2-D1	testis:	n/a
44	chr11:102221100-102221150	HCM	heart:	n/a
45	chr11:102221100-102221150	Caco-2	colon:	n/a
46	chr11:102221100-102221150	HCPEpiC	choroid plexus:	n/a
47	chr11:102221100-102221150	HRCEpiC	kidney:	n/a
48	chr11:102221100-102221150	HepG2	liver:	n/a
49	chr11:102221100-102221150	GM06990	blood:	n/a
50	chr11:102221100-102221150	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:102216212..102220028-chr11:102319803..102324997,8	K562	blood:
2	chr11:102217672..102219340-chr11:102322046..102323844,2	MCF-7	breast:
3	chr11:102187104..102190463-chr11:102217868..102220185,3	MCF-7	breast:
4	chr11:102216856..102220120-chr11:102221036..102226031,10	K562	blood:
5	chr11:102215215..102219130-chr11:102321135..102324493,6	K562	blood:
6	chr11:102217363..102222814-chr11:102227902..102233521,10	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BIRC2-1	chr11:102219329-102219744	NONHSAT023879
2	lnc-BIRC2-1	chr11:102219012-102219138	NONHSAT023879

Variant related genes	Relation type
BIRC2	TF binding region
BIRC2	CpG island
ENSG00000110330	chromatin interactions
ENSG00000152558	chromatin interactions
ENSG00000255337	chromatin interactions
ENSG00000023445	chromatin interactions

Extended variants
information (count: 129 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:129 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566479371	chr11:102219085-102219086	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
2	rs531982268	chr11:102219090-102219091	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
3	rs190716810	chr11:102219103-102219104	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
4	rs568932074	chr11:102219160-102219161	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs192831338	chr11:102219179-102219180	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs185213294	chr11:102219211-102219212	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs573527588	chr11:102219218-102219219	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs554848068	chr11:102219222-102219223	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs570183459	chr11:102219225-102219226	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs111506881	chr11:102219237-102219238	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs189037775	chr11:102219253-102219254	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs573195339	chr11:102219262-102219263	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs34262013	chr11:102219279-102219280	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs558521563	chr11:102219321-102219322	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs181177642	chr11:102219331-102219332	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
16	rs544278821	chr11:102219360-102219361	Weak transcription Flanking Active TSS Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
17	rs569260034	chr11:102219407-102219408	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
18	rs3210039	chr11:102219411-102219412	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
19	rs561182053	chr11:102219566-102219567	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
20	rs566399171	chr11:102219658-102219659	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
21	rs377016129	chr11:102219682-102219683	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
22	rs533874998	chr11:102219693-102219694	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs566515118	chr11:102219723-102219724	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
24	rs530200418	chr11:102219838-102219839	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs537924052	chr11:102219845-102219846	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs375629431	chr11:102219858-102219859	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs11604189	chr11:102219863-102219864	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs560577004	chr11:102219883-102219884	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs185519931	chr11:102219896-102219897	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs187973660	chr11:102219900-102219901	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs568864075	chr11:102219923-102219924	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs35669423	chr11:102219940-102219941	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs534170814	chr11:102219941-102219942	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs113213104	chr11:102219945-102219946	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs34014235	chr11:102220000-102220001	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs150461140	chr11:102220004-102220005	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs28364733	chr11:102220005-102220006	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs35522004	chr11:102220036-102220037	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs548289442	chr11:102220037-102220038	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs568275815	chr11:102220077-102220078	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs187057289	chr11:102220108-102220109	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs192229278	chr11:102220118-102220119	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs570700438	chr11:102220161-102220162	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs573052906	chr11:102220167-102220168	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs150746518	chr11:102220169-102220170	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs542087261	chr11:102220178-102220179	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs139036522	chr11:102220182-102220183	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs575218941	chr11:102220234-102220235	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555598099	chr11:102220252-102220253	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs35994698	chr11:102220256-102220257	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal cancer	21851588	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Colorectal cancer	16912164	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21720365	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102216200-102219600	Active TSS	A549	lung
2	chr11:102216400-102219200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:102216400-102219600	Active TSS	K562	blood
4	chr11:102216400-102219600	Active TSS	NHLF	lung
5	chr11:102216600-102219200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr11:102216600-102219200	Active TSS	Colonic Mucosa	Colon
7	chr11:102216600-102219200	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr11:102216600-102219400	Active TSS	Stomach Smooth Muscle	stomach
9	chr11:102216600-102219600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr11:102216600-102219600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:102216600-102219800	Active TSS	NHDF-Ad	bronchial
12	chr11:102216600-102220000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr11:102216600-102220200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr11:102216600-102220600	Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr11:102216800-102219200	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr11:102216800-102219200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
17	chr11:102216800-102219200	Active TSS	Aorta	Aorta
18	chr11:102216800-102219200	Active TSS	Fetal Muscle Trunk	muscle
19	chr11:102216800-102219200	Active TSS	Placenta Amnion	Placenta Amnion
20	chr11:102216800-102219400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:102216800-102219400	Active TSS	HSMMtube	muscle
22	chr11:102216800-102219400	Active TSS	Osteobl	bone
23	chr11:102216800-102219600	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr11:102216800-102219600	Active TSS	Fetal Brain Female	brain
25	chr11:102216800-102219600	Active TSS	HSMM	muscle
26	chr11:102216800-102220000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr11:102216800-102220000	Active TSS	Right Atrium	heart
28	chr11:102217000-102219200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:102217000-102219200	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr11:102217000-102219200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr11:102217000-102219200	Active TSS	Fetal Kidney	kidney
32	chr11:102217000-102219200	Active TSS	Placenta	Placenta
33	chr11:102217000-102219200	Active TSS	Left Ventricle	heart
34	chr11:102217000-102219200	Active TSS	Psoas Muscle	Psoas
35	chr11:102217000-102219200	Active TSS	Right Ventricle	heart
36	chr11:102217000-102219200	Active TSS	Small Intestine	intestine
37	chr11:102217000-102219400	Active TSS	Duodenum Mucosa	Duodenum
38	chr11:102217000-102219600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr11:102217000-102219600	Active TSS	Muscle Satellite Cultured Cells	--
40	chr11:102217000-102219600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr11:102217000-102219800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr11:102217000-102219800	Active TSS	Fetal Thymus	thymus
43	chr11:102217000-102220000	Active TSS	Thymus	Thymus
44	chr11:102217000-102221600	Active TSS	GM12878-XiMat	blood
45	chr11:102217200-102219200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr11:102217200-102219200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:102217200-102219200	Active TSS	H9 Cell Line	embryonic stem cell
48	chr11:102217200-102219200	Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr11:102217200-102219200	Active TSS	Primary T cells fromperipheralblood	blood
50	chr11:102217200-102219200	Active TSS	Primary T regulatory cells fromperipheralblood	blood

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