Variant report

Variant	nsv482158
Chromosome Location	chr11:17406798-17410206
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:428)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:344 , 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	BACH1	chr11:17408310-17408505	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr11:17408228-17408447	K562	blood:	n/a	n/a
3	CBX3	chr11:17408154-17408559	K562	blood:	n/a	n/a
4	CBX3	chr11:17408259-17408511	K562	blood:	n/a	n/a
5	CHD2	chr11:17408404-17408530	K562	blood:	n/a	n/a
6	CHD2	chr11:17408293-17408363	HepG2	liver:	n/a	n/a
7	CTCF	chr11:17407820-17407970	GM12873	blood:	n/a	n/a
8	CTCF	chr11:17410140-17410290	AG04449	skin:	n/a	n/a
9	CTCF	chr11:17408570-17408715	GM12891	blood:	n/a	n/a
10	CTCF	chr11:17408280-17408430	NHDF-neo	bronchial:	n/a	n/a
11	CTCF	chr11:17407520-17407670	SAEC	small airway:	n/a	n/a
12	CTCF	chr11:17408280-17408430	HRE	kidney:	n/a	n/a
13	CTCF	chr11:17408280-17408430	HMEC	breast:	n/a	n/a
14	CTCF	chr11:17407620-17407770	GM12873	blood:	n/a	n/a
15	CTCF	chr11:17408920-17409070	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr11:17408220-17408466	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr11:17408280-17408430	BJ	skin:	n/a	n/a
18	CTCF	chr11:17408302-17408393	Lung_OC	lung:	n/a	n/a
19	CTCF	chr11:17408260-17408410	GM12865	blood:	n/a	n/a
20	CTCF	chr11:17408260-17408410	GM12869	blood:	n/a	n/a
21	CTCF	chr11:17407660-17407810	RPTEC	kidney:	n/a	n/a
22	CTCF	chr11:17408260-17408410	GM12870	blood:	n/a	n/a
23	CTCF	chr11:17408230-17408493	GM10266	blood:	n/a	n/a
24	CTCF	chr11:17408230-17408496	MCF-7	breast:	n/a	n/a
25	CTCF	chr11:17408300-17408450	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr11:17409320-17409470	GM06990	blood:	n/a	n/a
27	CTCF	chr11:17408240-17408462	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr11:17408300-17408450	GM12871	blood:	n/a	n/a
29	CTCF	chr11:17408260-17408410	BJ	skin:	n/a	n/a
30	CTCF	chr11:17408188-17408533	GM19238	blood:	n/a	n/a
31	CTCF	chr11:17408720-17408870	GM12872	blood:	n/a	n/a
32	CTCF	chr11:17408280-17408430	HEK293	kidney:	n/a	n/a
33	CTCF	chr11:17408241-17408405	GM20000	blood:	n/a	n/a
34	CTCF	chr11:17408245-17408463	LNCaP	prostate:	n/a	n/a
35	CTCF	chr11:17408251-17408485	A549	lung:	n/a	n/a
36	CTCF	chr11:17408280-17408430	HL-60	blood:	n/a	n/a
37	CTCF	chr11:17408228-17408469	GM10248	blood:	n/a	n/a
38	CTCF	chr11:17408260-17408410	GM06990	blood:	n/a	n/a
39	CTCF	chr11:17408231-17408454	HepG2	liver:	n/a	n/a
40	CTCF	chr11:17408260-17408410	HPF	lung:	n/a	n/a
41	CTCF	chr11:17407900-17408050	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr11:17408576-17408585	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:17408240-17408390	GM12868	blood:	n/a	n/a
44	CTCF	chr11:17408203-17408504	GM19239	blood:	n/a	n/a
45	CTCF	chr11:17408460-17408610	GM12869	blood:	n/a	n/a
46	CTCF	chr11:17408260-17408410	GM12866	blood:	n/a	n/a
47	CTCF	chr11:17408175-17408509	A549	lung:	n/a	n/a
48	CTCF	chr11:17408280-17408430	HVMF	connective:	n/a	n/a
49	CTCF	chr11:17408651-17408698	ProgFib	skin:	n/a	n/a
50	CTCF	chr11:17408224-17408494	MCF-7	breast:	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	chr11:17410182-17410232	SK-N-SH_RA	brain:	n/a
2	chr11:17410182-17410232	SK-N-SH_RA	brain:	n/a
3	chr11:17409644-17409694	NHBE	bronchial:	n/a
4	chr11:17407432-17407482	AG04449	skin:	fetal
5	chr11:17408437-17408487	SKMC	muscle:	n/a
6	chr11:17409644-17409694	AG04450	lung:	fetal
7	chr11:17409188-17409238	HepG2	liver:	n/a
8	chr11:17409509-17409559	AG09319	gingival:	n/a
9	chr11:17409644-17409694	ovcar-3	ovarian:	n/a
10	chr11:17408437-17408487	AG09319	gingival:	n/a
11	chr11:17409602-17409652	MCF10A-Er-Src	breast:	n/a
12	chr11:17410182-17410232	HMEC	breast:	n/a
13	chr11:17409509-17409559	HCPEpiC	choroid plexus:	n/a
14	chr11:17409644-17409694	HUVEC	blood vessel:	n/a
15	chr11:17409602-17409652	SK-N-MC	brain:	n/a
16	chr11:17409644-17409694	ECC-1	luminal epithelium:	n/a
17	chr11:17409509-17409559	SK-N-SH	brain:	n/a
18	chr11:17409509-17409559	U87	brain:	n/a
19	chr11:17409644-17409694	SK-N-SH_RA	brain:	n/a
20	chr11:17410182-17410232	SK-N-SH	brain:	n/a
21	chr11:17409602-17409652	U87	brain:	n/a
22	chr11:17408437-17408487	LNCaP	prostate:	n/a
23	chr11:17408437-17408487	HCM	heart:	n/a
24	chr11:17408437-17408487	HMEC	breast:	n/a
25	chr11:17409509-17409559	GM19239	blood:	n/a
26	chr11:17409188-17409238	GM12891	blood:	n/a
27	chr11:17407432-17407482	HRPEpiC	eye:	n/a
28	chr11:17410182-17410232	Jurkat	blood:	n/a
29	chr11:17408437-17408487	SAEC	small airway:	n/a
30	chr11:17409644-17409694	HCPEpiC	choroid plexus:	n/a
31	chr11:17408437-17408487	AG10803	skin:	n/a
32	chr11:17407432-17407482	NT2-D1	testis:	n/a
33	chr11:17409188-17409238	HRPEpiC	eye:	n/a
34	chr11:17408437-17408487	HCF	heart:	n/a
35	chr11:17410182-17410232	NHBE	bronchial:	n/a
36	chr11:17410182-17410232	HepG2	liver:	n/a
37	chr11:17409644-17409694	Hepatocyte	liver:	n/a
38	chr11:17409644-17409694	NB4	blood:	n/a
39	chr11:17410182-17410232	Hepatocyte	liver:	n/a
40	chr11:17409644-17409694	GM19239	blood:	n/a
41	chr11:17408437-17408487	HCT-116	colon:	n/a
42	chr11:17410182-17410232	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:17409509-17409559	SK-N-SH_RA	brain:	n/a
44	chr11:17409644-17409694	HEK293	kidney:	embryo
45	chr11:17409188-17409238	Jurkat	blood:	n/a
46	chr11:17409644-17409694	ProgFib	skin:	n/a
47	chr11:17410182-17410232	GM19239	blood:	n/a
48	chr11:17407432-17407482	Jurkat	blood:	n/a
49	chr11:17410182-17410232	AG09309	skin:	n/a
50	chr11:17407432-17407482	H1-hESC	embryonic stem cell:	embryo

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17401527..17405179-chr11:17405771..17408702,5	K562	blood:
2	chr11:17407926..17410738-chr11:17427633..17429679,2	MCF-7	breast:
3	chr11:17405950..17408117-chr11:17411030..17412540,2	K562	blood:
4	chr11:17407664..17411994-chr11:17495609..17498712,4	MCF-7	breast:
5	chr11:17373252..17376530-chr11:17405235..17408726,4	K562	blood:
6	chr11:17409155..17411686-chr11:17415958..17417919,2	MCF-7	breast:
7	chr11:17407309..17407849-chr11:17525524..17526306,2	MCF-7	breast:
8	chr11:17373205..17377100-chr11:17409140..17413152,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC8-1	chr11:17407610-17407859	NONHSAT018231
2	lnc-ABCC8-1	chr11:17408130-17408297	NONHSAT018231

No data

Variant related genes	Relation type
KCNJ11	TF binding region
KCNJ11	CpG island
ENSG00000006071	chromatin interactions
ENSG00000260196	chromatin interactions
ENSG00000188211	chromatin interactions

Extended variants
information (count: 199 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:199 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563531727	chr11:17406813-17406814	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs569684578	chr11:17406890-17406891	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs569535045	chr11:17406911-17406912	Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs537326228	chr11:17407037-17407038	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs191682072	chr11:17407269-17407270	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs74831871	chr11:17407284-17407285	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs76774792	chr11:17407285-17407286	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs573875884	chr11:17407288-17407289	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs182349583	chr11:17407298-17407299	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35749958	chr11:17407328-17407329	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs191697899	chr11:17407334-17407335	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs553139186	chr11:17407343-17407344	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs572399316	chr11:17407412-17407413	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs528111410	chr11:17407432-17407433	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564292096	chr11:17407433-17407434	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531631096	chr11:17407451-17407452	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs5205	chr11:17407477-17407478	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs562092401	chr11:17407549-17407550	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs186637027	chr11:17407561-17407562	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs529436579	chr11:17407566-17407567	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs372136553	chr11:17407596-17407597	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs547635594	chr11:17407604-17407605	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs5206	chr11:17407618-17407619	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs372655579	chr11:17407639-17407640	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs193101892	chr11:17407700-17407701	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs543277374	chr11:17407727-17407728	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs561545376	chr11:17407750-17407751	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs5207	chr11:17407765-17407766	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs117976105	chr11:17407769-17407770	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs147282653	chr11:17407780-17407781	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs185669328	chr11:17407877-17407878	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs555689354	chr11:17407901-17407902	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs567523345	chr11:17407902-17407903	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs534917931	chr11:17407908-17407909	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs115826080	chr11:17407937-17407938	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs377292224	chr11:17407938-17407939	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs79457490	chr11:17407979-17407980	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs369186082	chr11:17408010-17408011	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs2285676	chr11:17408025-17408026	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs35294169	chr11:17408030-17408031	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs148712397	chr11:17408032-17408033	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs576026175	chr11:17408063-17408064	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs5208	chr11:17408090-17408091	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs561755715	chr11:17408106-17408107	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs529498937	chr11:17408107-17408108	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs372737066	chr11:17408129-17408130	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs541725017	chr11:17408130-17408131	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs118179872	chr11:17408131-17408132	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs533601283	chr11:17408147-17408148	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs5209	chr11:17408178-17408179	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	21865298	CNVD

Chromatin state (count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17394200-17407600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr11:17394400-17410200	Weak transcription	A549	lung
3	chr11:17395200-17410200	Weak transcription	Thymus	Thymus
4	chr11:17395600-17410200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr11:17395600-17410400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr11:17395800-17409200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr11:17396000-17408800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:17396600-17410200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr11:17397200-17407800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr11:17398200-17410200	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr11:17398800-17410200	Weak transcription	Primary T cells from cord blood	blood
12	chr11:17400600-17408000	Strong transcription	Fetal Intestine Small	intestine
13	chr11:17400600-17408800	Weak transcription	Brain Germinal Matrix	brain
14	chr11:17400800-17407200	Weak transcription	Fetal Brain Female	brain
15	chr11:17400800-17410200	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr11:17401000-17410200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr11:17401200-17407200	Weak transcription	Lung	lung
18	chr11:17401600-17410200	Weak transcription	Hela-S3	cervix
19	chr11:17401600-17410200	Weak transcription	K562	blood
20	chr11:17401800-17407400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr11:17401800-17407400	Weak transcription	HepG2	liver
22	chr11:17401800-17410200	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr11:17402000-17410200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:17402000-17410200	Weak transcription	HMEC	breast
25	chr11:17402400-17407800	Weak transcription	Fetal Intestine Large	intestine
26	chr11:17403000-17410400	Weak transcription	Aorta	Aorta
27	chr11:17403600-17408600	Weak transcription	Duodenum Mucosa	Duodenum
28	chr11:17403800-17410400	Weak transcription	HSMMtube	muscle
29	chr11:17404000-17408000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr11:17404200-17410200	Weak transcription	HSMM	muscle
31	chr11:17404400-17407600	Weak transcription	Right Atrium	heart
32	chr11:17405000-17408600	Enhancers	Brain Angular Gyrus	brain
33	chr11:17405200-17407400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr11:17405200-17412000	Enhancers	Fetal Brain Male	brain
35	chr11:17405400-17407000	Enhancers	Fetal Muscle Trunk	muscle
36	chr11:17405400-17407000	Enhancers	Psoas Muscle	Psoas
37	chr11:17405400-17407200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr11:17405400-17407600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr11:17405400-17408200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
40	chr11:17405400-17409800	Transcr. at gene 5' and 3'	Dnd41	blood
41	chr11:17405600-17407200	Weak transcription	Fetal Heart	heart
42	chr11:17405600-17407200	Enhancers	Fetal Muscle Leg	muscle
43	chr11:17405600-17408800	Weak transcription	Esophagus	oesophagus
44	chr11:17405600-17409200	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
45	chr11:17406000-17407200	Weak transcription	Left Ventricle	heart
46	chr11:17406000-17407800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:17406000-17408800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr11:17406000-17410200	Weak transcription	Brain Hippocampus Middle	brain
49	chr11:17406200-17406800	Strong transcription	Gastric	stomach
50	chr11:17406200-17407400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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