Variant report

Variant	nsv526778
Chromosome Location	chr11:9159739-9185077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:338)
CpG islands
(count:123)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr11:9160361-9160994	HCT-116	colon:	n/a	n/a
2	CEBPB	chr11:9183604-9183789	HepG2	liver:	n/a	chr11:9183742-9183753 chr11:9183715-9183726
3	CEBPB	chr11:9182901-9183105	IMR90	lung:	n/a	chr11:9182961-9182972
4	CEBPB	chr11:9180345-9180857	HepG2	liver:	n/a	chr11:9180469-9180480
5	CEBPB	chr11:9160548-9160786	IMR90	lung:	n/a	n/a
6	CEBPB	chr11:9183632-9183779	IMR90	lung:	n/a	chr11:9183742-9183753 chr11:9183715-9183726
7	CEBPB	chr11:9180329-9181012	Hela-S3	cervix:	n/a	chr11:9180469-9180480
8	CEBPB	chr11:9180341-9180662	K562	blood:	n/a	chr11:9180469-9180480
9	CEBPB	chr11:9180288-9180843	K562	blood:	n/a	chr11:9180469-9180480
10	CEBPB	chr11:9180308-9180914	A549	lung:	n/a	chr11:9180469-9180480
11	CEBPB	chr11:9180300-9181026	IMR90	lung:	n/a	chr11:9180469-9180480
12	CEBPB	chr11:9180462-9181042	HCT-116	colon:	n/a	chr11:9180469-9180480
13	CEBPB	chr11:9160485-9160863	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:9182818-9183108	HepG2	liver:	n/a	chr11:9182961-9182972
15	CEBPB	chr11:9183624-9183790	A549	lung:	n/a	chr11:9183742-9183753 chr11:9183715-9183726
16	CEBPB	chr11:9180550-9180783	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr11:9180342-9180912	A549	lung:	n/a	chr11:9180469-9180480
18	CHD2	chr11:9160512-9160899	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr11:9160594-9160780	A549	lung:	n/a	n/a
20	CTCF	chr11:9159900-9160170	BJ	skin:	n/a	n/a
21	CTCF	chr11:9159016-9159909	SK-N-SH	brain:	n/a	n/a
22	CTCF	chr11:9159760-9159910	GM12871	blood:	n/a	n/a
23	CTCF	chr11:9160280-9160430	HPAF	blood vessel:	n/a	n/a
24	CTCF	chr11:9166782-9166845	GM12892	blood:	n/a	n/a
25	CTCF	chr11:9160100-9160250	HRE	kidney:	n/a	n/a
26	CTCF	chr11:9171900-9172050	K562	blood:	n/a	n/a
27	CTCF	chr11:9159700-9159850	GM12869	blood:	n/a	n/a
28	CTCF	chr11:9159740-9159890	SAEC	small airway:	n/a	n/a
29	CTCF	chr11:9172560-9172710	HPAF	blood vessel:	n/a	n/a
30	CTCF	chr11:9159800-9159950	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr11:9159767-9159805	NHEK	skin:	n/a	n/a
32	CTCF	chr11:9159742-9159858	GM12892	blood:	n/a	n/a
33	CTCF	chr11:9159720-9159870	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr11:9160900-9161050	Caco-2	colon:	n/a	n/a
35	CTCF	chr11:9160160-9160310	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr11:9169340-9169490	GM12864	blood:	n/a	n/a
37	CTCF	chr11:9159780-9159930	GM12868	blood:	n/a	n/a
38	CTCF	chr11:9166763-9166856	GM19240	blood:	n/a	n/a
39	CTCF	chr11:9166760-9166910	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr11:9160900-9161050	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr11:9160160-9160310	GM12867	blood:	n/a	n/a
42	CTCF	chr11:9165780-9165930	GM12865	blood:	n/a	chr11:9165860-9165873
43	CTCF	chr11:9159188-9159830	HCT-116	colon:	n/a	n/a
44	CTCF	chr11:9161351-9161380	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr11:9160160-9160310	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr11:9159940-9160090	K562	blood:	n/a	n/a
47	CTCF	chr11:9166841-9166907	GM12878	blood:	n/a	n/a
48	CTCF	chr11:9172600-9172750	HCFaa	heart:	n/a	n/a
49	CTCF	chr11:9159750-9159819	GM19239	blood:	n/a	n/a
50	CTCF	chr11:9159741-9159843	GM19238	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9172290-9172340	NH-A	brain:	n/a
2	chr11:9172290-9172340	NH-A	brain:	n/a
3	chr11:9172290-9172340	SK-N-SH	brain:	n/a
4	chr11:9172290-9172340	AG04450	lung:	fetal
5	chr11:9172290-9172340	AG09319	gingival:	n/a
6	chr11:9160869-9160919	AG09319	gingival:	n/a
7	chr11:9160869-9160919	PFSK-1	brain:	n/a
8	chr11:9172290-9172340	MCF10A-Er-Src	breast:	n/a
9	chr11:9172290-9172340	HEEpiC	esophagus:	n/a
10	chr11:9172290-9172340	Jurkat	blood:	n/a
11	chr11:9160869-9160919	K562	blood:	n/a
12	chr11:9160869-9160919	HIPEpiC	eye:	n/a
13	chr11:9172290-9172340	AoSMC	blood vessel:	n/a
14	chr11:9160869-9160919	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:9160869-9160919	NB4	blood:	n/a
16	chr11:9160869-9160919	ProgFib	skin:	n/a
17	chr11:9160869-9160919	NT2-D1	testis:	n/a
18	chr11:9160869-9160919	NHDF-neo	bronchial:	n/a
19	chr11:9160869-9160919	BJ	skin:	n/a
20	chr11:9172290-9172340	T-47D	breast:	n/a
21	chr11:9160869-9160919	PrEC	prostate:	n/a
22	chr11:9172290-9172340	PANC-1	pancreas:	n/a
23	chr11:9160869-9160919	BE2_C	brain:	n/a
24	chr11:9160869-9160919	HUVEC	blood vessel:	n/a
25	chr11:9172290-9172340	SKMC	muscle:	n/a
26	chr11:9172290-9172340	LNCaP	prostate:	n/a
27	chr11:9160869-9160919	IMR90	lung:	fetal
28	chr11:9172290-9172340	HNPCEpiC	eye:	n/a
29	chr11:9172290-9172340	Caco-2	colon:	n/a
30	chr11:9160869-9160919	GM12892	blood:	n/a
31	chr11:9172290-9172340	SAEC	small airway:	n/a
32	chr11:9160869-9160919	HCPEpiC	choroid plexus:	n/a
33	chr11:9160869-9160919	ovcar-3	ovarian:	n/a
34	chr11:9172290-9172340	AG10803	skin:	n/a
35	chr11:9172290-9172340	GM12892	blood:	n/a
36	chr11:9160869-9160919	HepG2	liver:	n/a
37	chr11:9172290-9172340	AG04449	skin:	fetal
38	chr11:9172290-9172340	GM06990	blood:	n/a
39	chr11:9160869-9160919	HMEC	breast:	n/a
40	chr11:9160869-9160919	MCF-7	breast:	n/a
41	chr11:9160869-9160919	GM12891	blood:	n/a
42	chr11:9160869-9160919	HCM	heart:	n/a
43	chr11:9160869-9160919	HNPCEpiC	eye:	n/a
44	chr11:9172290-9172340	PFSK-1	brain:	n/a
45	chr11:9172290-9172340	HepG2	liver:	n/a
46	chr11:9172290-9172340	BJ	skin:	n/a
47	chr11:9160869-9160919	LNCaP	prostate:	n/a
48	chr11:9172290-9172340	HCF	heart:	n/a
49	chr11:9160869-9160919	NH-A	brain:	n/a
50	chr11:9160869-9160919	HCF	heart:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:8983863..8986997-chr11:9158044..9162292,6	MCF-7	breast:
2	chr11:9041862..9044730-chr11:9157486..9160225,2	MCF-7	breast:
3	chr11:9169410..9173680-chr11:9196051..9200398,3	MCF-7	breast:
4	chr11:9108929..9110845-chr11:9168410..9170250,2	MCF-7	breast:
5	chr11:9036789..9038692-chr11:9159866..9161634,2	MCF-7	breast:
6	chr11:9164117..9168373-chr11:9169082..9171685,4	K562	blood:
7	chr11:9108004..9116385-chr11:9156452..9162678,21	MCF-7	breast:
8	chr11:9166569..9169771-chr11:9171907..9174978,4	K562	blood:
9	chr11:9173577..9175591-chr11:9176110..9178971,2	K562	blood:
10	chr11:9163547..9165539-chr11:9168849..9171876,3	K562	blood:
11	chr11:9163288..9165423-chr11:9175332..9177316,2	MCF-7	breast:
12	chr11:9164859..9166403-chr11:9483116..9485555,2	K562	blood:
13	chr11:9182254..9183881-chr11:9184543..9187161,2	K562	blood:
14	chr11:9173577..9175591-chr11:9176110..9178971,3	K562	blood:
15	chr11:9109700..9116224-chr11:9155740..9163743,14	MCF-7	breast:
16	chr11:9166569..9169771-chr11:9171907..9174978,4	K562	blood:
17	chr11:9163547..9165539-chr11:9168849..9171876,3	K562	blood:
18	chr11:9182254..9183881-chr11:9184543..9187161,2	K562	blood:
19	chr11:9182922..9186858-chr11:9284240..9287968,3	K562	blood:

No data

Variant related genes	Relation type
DENND5A	TF binding region
SCUBE2	TF binding region
DENND5A	CpG island
SCUBE2	CpG island
ENSG00000254860	chromatin interactions
ENSG00000175348	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000213538	chromatin interactions
ENSG00000175356	chromatin interactions
ENSG00000184014	chromatin interactions
ENSG00000264984	chromatin interactions

Extended variants
information (count: 962 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:962 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7396512	chr11:9159739-9159740	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112629686	chr11:9159747-9159748	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs181625491	chr11:9159749-9159750	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs561026846	chr11:9159758-9159759	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs73416044	chr11:9159775-9159776	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs370445624	chr11:9159807-9159808	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs1353729	chr11:9159818-9159819	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs532169617	chr11:9159873-9159874	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs186288990	chr11:9159907-9159908	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs192020093	chr11:9159938-9159939	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs113471211	chr11:9159940-9159941	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs149375108	chr11:9159955-9159956	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs568641512	chr11:9159958-9159959	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs144698293	chr11:9159972-9159973	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs552322501	chr11:9160009-9160010	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs370169989	chr11:9160024-9160025	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs1353730	chr11:9160070-9160071	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs576797905	chr11:9160078-9160079	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs539474825	chr11:9160086-9160087	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs558413955	chr11:9160191-9160192	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs572047400	chr11:9160195-9160196	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs540821958	chr11:9160219-9160220	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs560870315	chr11:9160226-9160227	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs535026312	chr11:9160231-9160232	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs574581792	chr11:9160258-9160259	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs543125550	chr11:9160261-9160262	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs187531245	chr11:9160282-9160283	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs554852424	chr11:9160295-9160296	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs545858142	chr11:9160322-9160323	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs574745549	chr11:9160326-9160327	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs191215331	chr11:9160425-9160426	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs182506810	chr11:9160466-9160467	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs61877786	chr11:9160486-9160487	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs117344697	chr11:9160523-9160524	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	mRNA abundance
35	rs201695191	chr11:9160526-9160527	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs568526544	chr11:9160546-9160547	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs11558094	chr11:9160552-9160553	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs111360702	chr11:9160586-9160587	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs377753608	chr11:9160587-9160588	Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs187059248	chr11:9160603-9160604	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs148092168	chr11:9160629-9160630	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs570645255	chr11:9160668-9160669	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs370436200	chr11:9160691-9160692	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs559129546	chr11:9160708-9160709	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs143798117	chr11:9160763-9160764	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs16906742	chr11:9160766-9160767	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs554861372	chr11:9160788-9160789	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs574526929	chr11:9160795-9160796	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs543638491	chr11:9160802-9160803	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs541803005	chr11:9160820-9160821	Genic enhancers Enhancers Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1011 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9113600-9159800	Weak transcription	Right Ventricle	heart
2	chr11:9134800-9161200	Weak transcription	Fetal Brain Male	brain
3	chr11:9142400-9163000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr11:9142600-9175000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:9143400-9161200	Weak transcription	Aorta	Aorta
6	chr11:9144400-9161200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:9150600-9160000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr11:9151800-9160800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:9151800-9175800	Strong transcription	Fetal Muscle Trunk	muscle
10	chr11:9152000-9159800	Weak transcription	Liver	Liver
11	chr11:9152200-9160600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:9152600-9160200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:9152800-9175800	Strong transcription	Fetal Muscle Leg	muscle
14	chr11:9153000-9160200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:9153000-9179800	Strong transcription	Monocytes-CD14+_RO01746	blood
16	chr11:9153600-9160600	Weak transcription	Colon Smooth Muscle	Colon
17	chr11:9153600-9164400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr11:9154200-9160000	Weak transcription	Left Ventricle	heart
19	chr11:9154600-9160000	Strong transcription	HSMM	muscle
20	chr11:9154600-9160600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr11:9155000-9163000	Weak transcription	Psoas Muscle	Psoas
22	chr11:9155000-9203400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:9155600-9161200	Weak transcription	Fetal Kidney	kidney
24	chr11:9156000-9163000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:9156800-9167200	Strong transcription	Placenta	Placenta
26	chr11:9157000-9160000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:9157000-9180000	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr11:9157200-9159800	Strong transcription	NHLF	lung
29	chr11:9157400-9160800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr11:9158000-9183200	Strong transcription	Primary neutrophils fromperipheralblood	blood
31	chr11:9158400-9159800	Genic enhancers	Brain Cingulate Gyrus	brain
32	chr11:9158400-9160200	Strong transcription	HSMMtube	muscle
33	chr11:9158400-9160800	Enhancers	Pancreas	Pancrea
34	chr11:9158400-9161000	Enhancers	Gastric	stomach
35	chr11:9158400-9164600	Strong transcription	GM12878-XiMat	blood
36	chr11:9158600-9160200	Strong transcription	Fetal Stomach	stomach
37	chr11:9158600-9165600	Strong transcription	Primary hematopoietic stem cells	blood
38	chr11:9158800-9159800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:9158800-9160000	Genic enhancers	Brain Angular Gyrus	brain
40	chr11:9158800-9160800	Enhancers	Colonic Mucosa	Colon
41	chr11:9158800-9161200	Enhancers	Stomach Mucosa	stomach
42	chr11:9158800-9161800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:9158800-9162400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr11:9158800-9162400	Genic enhancers	A549	lung
45	chr11:9158800-9162600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr11:9158800-9165000	Strong transcription	Fetal Brain Female	brain
47	chr11:9158800-9166400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr11:9158800-9166600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr11:9159000-9159800	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr11:9159000-9159800	Genic enhancers	Adipose Nuclei	Adipose

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