Variant report

Variant	nsv897922
Chromosome Location	chr11:75116733-75147661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1692)
CpG islands
(count:1894)
Chromatin interactive
region (count:90)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1692 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:75118941-75119277	K562	blood:	n/a	n/a
2	ARID3A	chr11:75117339-75117736	K562	blood:	n/a	n/a
3	ARID3A	chr11:75139279-75139495	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:75133190-75133992	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:75118863-75119285	HepG2	liver:	n/a	n/a
6	ATF2	chr11:75119235-75119631	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:75118785-75119193	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr11:75118872-75119220	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:75118962-75119100	K562	blood:	n/a	n/a
10	BACH1	chr11:75141002-75141723	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:75136661-75136817	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr11:75119746-75120203	A549	lung:	n/a	n/a
13	BCL3	chr11:75118680-75119356	A549	lung:	n/a	n/a
14	BCL3	chr11:75133147-75133915	A549	lung:	n/a	n/a
15	BCL3	chr11:75117307-75118158	K562	blood:	n/a	n/a
16	BCL3	chr11:75133011-75133759	A549	lung:	n/a	n/a
17	BCL3	chr11:75118687-75119470	K562	blood:	n/a	n/a
18	BCL3	chr11:75129819-75130368	A549	lung:	n/a	n/a
19	BCLAF1	chr11:75117060-75118115	K562	blood:	n/a	n/a
20	BCLAF1	chr11:75117279-75117954	K562	blood:	n/a	n/a
21	BCLAF1	chr11:75118726-75119349	GM12878	blood:	n/a	n/a
22	BHLHE40	chr11:75140889-75140992	GM12878	blood:	n/a	n/a
23	BHLHE40	chr11:75117344-75117667	K562	blood:	n/a	n/a
24	BHLHE40	chr11:75133720-75134022	K562	blood:	n/a	n/a
25	BHLHE40	chr11:75118964-75119164	GM12878	blood:	n/a	n/a
26	BHLHE40	chr11:75131423-75131608	K562	blood:	n/a	n/a
27	BHLHE40	chr11:75131839-75132344	K562	blood:	n/a	chr11:75131929-75131938
28	BRCA1	chr11:75141816-75142070	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr11:75141424-75141430	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr11:75131268-75131697	K562	blood:	n/a	n/a
31	CCNT2	chr11:75131298-75131623	K562	blood:	n/a	n/a
32	CCNT2	chr11:75117250-75117843	K562	blood:	n/a	n/a
33	CCNT2	chr11:75131941-75132659	K562	blood:	n/a	chr11:75132176-75132196
34	CCNT2	chr11:75133566-75134031	K562	blood:	n/a	chr11:75133873-75133893
35	CEBPB	chr11:75129864-75130357	A549	lung:	n/a	n/a
36	CEBPB	chr11:75130053-75130376	A549	lung:	n/a	n/a
37	CEBPB	chr11:75117240-75117699	K562	blood:	n/a	n/a
38	CEBPB	chr11:75136740-75136919	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr11:75133042-75133680	A549	lung:	n/a	n/a
40	CEBPB	chr11:75129940-75130433	IMR90	lung:	n/a	n/a
41	CEBPB	chr11:75130064-75130420	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:75133049-75133699	A549	lung:	n/a	n/a
43	CEBPB	chr11:75125191-75125388	HepG2	liver:	n/a	chr11:75125269-75125282 chr11:75125270-75125281
44	CEBPB	chr11:75118960-75119159	K562	blood:	n/a	n/a
45	CEBPB	chr11:75129960-75130390	A549	lung:	n/a	n/a
46	CEBPD	chr11:75117219-75117762	K562	blood:	n/a	n/a
47	CEBPD	chr11:75131987-75132464	K562	blood:	n/a	n/a
48	CEBPD	chr11:75117197-75117800	K562	blood:	n/a	n/a
49	CEBPD	chr11:75131938-75132461	K562	blood:	n/a	n/a
50	CHD2	chr11:75136633-75136833	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75141815-75141865	Caco-2	colon:	n/a
2	chr11:75135383-75135433	HMEC	breast:	n/a
3	chr11:75141815-75141865	MCF-7	breast:	n/a
4	chr11:75141815-75141865	Caco-2	colon:	n/a
5	chr11:75135383-75135433	HMEC	breast:	n/a
6	chr11:75141815-75141865	MCF-7	breast:	n/a
7	chr11:75141627-75141677	HRPEpiC	eye:	n/a
8	chr11:75140541-75140591	Jurkat	blood:	n/a
9	chr11:75132468-75132518	SK-N-SH	brain:	n/a
10	chr11:75133593-75133643	GM12878	blood:	n/a
11	chr11:75136839-75136889	SKMC	muscle:	n/a
12	chr11:75133593-75133643	CMK	blood:	n/a
13	chr11:75141722-75141772	T-47D	breast:	n/a
14	chr11:75141835-75141885	HRE	kidney:	n/a
15	chr11:75141967-75142017	GM12891	blood:	n/a
16	chr11:75135383-75135433	HCF	heart:	n/a
17	chr11:75139544-75139594	ProgFib	skin:	n/a
18	chr11:75136655-75136705	GM19239	blood:	n/a
19	chr11:75142012-75142062	HEEpiC	esophagus:	n/a
20	chr11:75135383-75135433	AG04450	lung:	fetal
21	chr11:75140541-75140591	LNCaP	prostate:	n/a
22	chr11:75139390-75139440	CMK	blood:	n/a
23	chr11:75141815-75141865	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:75146471-75146521	HRCEpiC	kidney:	n/a
25	chr11:75132468-75132518	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:75139736-75139786	GM12891	blood:	n/a
27	chr11:75140865-75140915	H1-hESC	embryonic stem cell:	embryo
28	chr11:75141967-75142017	HRCEpiC	kidney:	n/a
29	chr11:75140865-75140915	PFSK-1	brain:	n/a
30	chr11:75143724-75143774	SKMC	muscle:	n/a
31	chr11:75142012-75142062	LNCaP	prostate:	n/a
32	chr11:75141627-75141677	U87	brain:	n/a
33	chr11:75144708-75144758	A549	lung:	n/a
34	chr11:75144708-75144758	NHDF-neo	bronchial:	n/a
35	chr11:75140541-75140591	AG04450	lung:	fetal
36	chr11:75142449-75142499	T-47D	breast:	n/a
37	chr11:75140681-75140731	AG09319	gingival:	n/a
38	chr11:75141735-75141785	GM19239	blood:	n/a
39	chr11:75141967-75142017	A549	lung:	n/a
40	chr11:75141793-75141843	RPTEC	kidney:	n/a
41	chr11:75141815-75141865	HEK293	kidney:	embryo
42	chr11:75141846-75141896	MCF-7	breast:	n/a
43	chr11:75141846-75141896	HCT-116	colon:	n/a
44	chr11:75141735-75141785	HUVEC	blood vessel:	n/a
45	chr11:75130069-75130119	HRPEpiC	eye:	n/a
46	chr11:75141722-75141772	HAEpiC	amniotic membrane:	n/a
47	chr11:75141846-75141896	AG04449	skin:	fetal
48	chr11:75140865-75140915	ovcar-3	ovarian:	n/a
49	chr11:75139736-75139786	HMEC	breast:	n/a
50	chr11:75146471-75146521	HIPEpiC	eye:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:75040053..75042610-chr11:75118135..75119953,2	K562	blood:
2	chr11:75132514..75134087-chr11:75134186..75136176,2	K562	blood:
3	chr11:75109502..75112547-chr11:75141371..75143241,3	K562	blood:
4	chr11:75136695..75138362-chr11:75139992..75142963,2	K562	blood:
5	chr11:75116986..75119499-chr11:75235046..75238810,4	K562	blood:
6	chr11:75122124..75127716-chr11:75129624..75133072,6	MCF-7	breast:
7	chr11:75124911..75127716-chr11:75131306..75134376,3	K562	blood:
8	chr11:75115551..75117959-chr11:75139316..75141039,2	K562	blood:
9	chr11:75110683..75112294-chr11:75142626..75145319,2	MCF-7	breast:
10	chr11:75035911..75038821-chr11:75120189..75122364,2	MCF-7	breast:
11	chr11:75116302..75120034-chr11:75143308..75145079,3	MCF-7	breast:
12	chr11:74970676..74972225-chr11:75133212..75135335,2	K562	blood:
13	chr11:75146374..75149145-chr11:75235740..75238570,3	MCF-7	breast:
14	chr11:75141213..75141791-chr6:116421902..116422557,2	Hela-S3	cervix:
15	chr11:75136185..75138324-chr11:75272295..75274643,2	MCF-7	breast:
16	chr11:75121805..75124460-chr11:75124847..75127735,2	K562	blood:
17	chr11:75116825..75117472-chr4:144105554..144106346,2	NB4	blood:
18	chr11:74991174..74992022-chr11:75133209..75133801,2	MCF-7	breast:
19	chr1:229644154..229644759-chr11:75140868..75141602,2	Hela-S3	cervix:
20	chr11:75132514..75134087-chr11:75134186..75136176,2	K562	blood:
21	chr11:75053294..75054862-chr11:75117237..75118876,2	MCF-7	breast:
22	chr11:75122268..75124877-chr11:75130912..75134393,4	K562	blood:
23	chr11:75116817..75118910-chr11:75131557..75134243,2	K562	blood:
24	chr11:75147641..75149262-chr12:53295951..53297582,2	MCF-7	breast:
25	chr1:147806617..147807147-chr11:75140408..75141165,2	Hela-S3	cervix:
26	chr11:75123559..75127434-chr11:75138022..75142436,6	MCF-7	breast:
27	chr11:75115551..75117959-chr11:75139316..75141039,2	K562	blood:
28	chr11:75130108..75133547-chr11:75244379..75247630,4	K562	blood:
29	chr11:75118946..75121248-chr11:75242299..75245442,3	K562	blood:
30	chr11:75141246..75141914-chr17:35715699..35716679,2	Hela-S3	cervix:
31	chr11:75127472..75131513-chr11:75141648..75144922,3	K562	blood:
32	chr11:75124995..75127197-chr11:75130235..75131924,2	K562	blood:
33	chr11:75111782..75113849-chr11:75133986..75135853,2	K562	blood:
34	chr11:75109263..75112751-chr11:75131805..75136633,9	MCF-7	breast:
35	chr11:75147262..75148920-chr11:75157020..75159435,2	K562	blood:
36	chr11:75109640..75112257-chr11:75126365..75128955,3	MCF-7	breast:
37	chr11:75125667..75127320-chr11:75132876..75135732,2	K562	blood:
38	chr11:75143358..75145748-chr11:75275231..75276876,2	MCF-7	breast:
39	chr11:75137530..75143776-chr11:75234822..75239544,9	MCF-7	breast:
40	chr11:75115990..75119066-chr11:75236154..75238810,3	K562	blood:
41	chr11:75121805..75124577-chr11:75124847..75127280,2	K562	blood:
42	chr11:75132815..75134620-chr11:75156705..75159268,2	K562	blood:
43	chr11:75099560..75100493-chr11:75135976..75137295,5	K562	blood:
44	chr11:75122807..75124831-chr11:75127769..75130348,4	K562	blood:
45	chr11:75017821..75020179-chr11:75116182..75118879,2	MCF-7	breast:
46	chr11:75109502..75112547-chr11:75141371..75144789,4	K562	blood:
47	chr11:75137733..75142671-chr11:75143548..75147382,7	K562	blood:
48	chr11:75122124..75127716-chr11:75129624..75133072,6	MCF-7	breast:
49	chr11:75122940..75124831-chr11:75127769..75129373,2	K562	blood:
50	chr11:75128783..75131051-chr11:75135705..75137919,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL35-3	chr11:75147150-75147336	ucscGeneNc_uc001owz_2

No data

Variant related genes	Relation type
KLHL35	TF binding region
KLHL35	CpG island
ENSG00000149273	chromatin interactions
ENSG00000198382	chromatin interactions
ENSG00000254429	chromatin interactions
ENSG00000250326	chromatin interactions
ENSG00000124145	chromatin interactions
ENSG00000207445	chromatin interactions
ENSG00000158555	chromatin interactions
ENSG00000149257	chromatin interactions
ENSG00000206941	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000223635	chromatin interactions
ENSG00000170185	chromatin interactions
ENSG00000149243	chromatin interactions
ENSG00000132142	chromatin interactions
ENSG00000255507	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000202408	chromatin interactions
ENSG00000178425	chromatin interactions

Extended variants
information (count: 1281 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113077609	chr11:75116733-75116734	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs534790024	chr11:75116811-75116812	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs553591383	chr11:75116822-75116823	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs576203355	chr11:75116852-75116853	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs35287469	chr11:75116894-75116895	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs17881991	chr11:75116901-75116902	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs4556572	chr11:75116953-75116954	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs4348932	chr11:75116959-75116960	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs373250720	chr11:75116996-75116997	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs113326571	chr11:75117003-75117004	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs547500846	chr11:75117004-75117005	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs146526678	chr11:75117049-75117050	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs112084193	chr11:75117059-75117060	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs7123178	chr11:75117074-75117075	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs569074088	chr11:75117077-75117078	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs139188001	chr11:75117088-75117089	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs554590475	chr11:75117093-75117094	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs184601455	chr11:75117105-75117106	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs568307777	chr11:75117118-75117119	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs534074991	chr11:75117157-75117158	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs377137847	chr11:75117183-75117184	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs553523072	chr11:75117250-75117251	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs576742020	chr11:75117254-75117255	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs368212968	chr11:75117271-75117272	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs141510920	chr11:75117302-75117303	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs12288089	chr11:75117303-75117304	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs75563460	chr11:75117306-75117307	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs372129459	chr11:75117316-75117317	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs17879451	chr11:75117353-75117354	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562305410	chr11:75117403-75117404	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs572683678	chr11:75117522-75117523	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541674780	chr11:75117543-75117544	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564345276	chr11:75117569-75117570	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533317830	chr11:75117669-75117670	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138310514	chr11:75117701-75117702	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs576254954	chr11:75117730-75117731	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs563809869	chr11:75117776-75117777	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs17879240	chr11:75117911-75117912	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188521284	chr11:75117966-75117967	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181290477	chr11:75117981-75117982	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs568547236	chr11:75117987-75117988	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549913489	chr11:75117996-75117997	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548110437	chr11:75117997-75117998	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs543051472	chr11:75118001-75118002	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564869052	chr11:75118071-75118072	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533861476	chr11:75118078-75118079	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149646945	chr11:75118124-75118125	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs3094304	chr11:75118158-75118159	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs570359514	chr11:75118160-75118161	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539007160	chr11:75118165-75118166	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1842 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75112400-75117600	Strong transcription	Rectal Smooth Muscle	rectum
2	chr11:75112400-75120200	Strong transcription	Stomach Smooth Muscle	stomach
3	chr11:75112600-75116800	Genic enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr11:75112600-75117000	Strong transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr11:75112600-75117000	Strong transcription	Right Ventricle	heart
6	chr11:75112600-75117600	Strong transcription	Brain Cingulate Gyrus	brain
7	chr11:75112600-75120000	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr11:75112800-75117400	Strong transcription	Brain Angular Gyrus	brain
9	chr11:75112800-75120200	Strong transcription	Brain Inferior Temporal Lobe	brain
10	chr11:75113000-75118200	Strong transcription	Aorta	Aorta
11	chr11:75113000-75118200	Strong transcription	Ovary	ovary
12	chr11:75113200-75117600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr11:75113200-75118200	Strong transcription	Duodenum Smooth Muscle	Duodenum
14	chr11:75113200-75118400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:75113200-75118400	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr11:75113200-75118400	Strong transcription	Colon Smooth Muscle	Colon
17	chr11:75113200-75120200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr11:75113200-75120200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:75113200-75120400	Strong transcription	Placenta	Placenta
20	chr11:75113400-75117600	Strong transcription	Esophagus	oesophagus
21	chr11:75113400-75117600	Genic enhancers	NHLF	lung
22	chr11:75113400-75118000	Strong transcription	Brain Hippocampus Middle	brain
23	chr11:75113400-75118200	Strong transcription	Left Ventricle	heart
24	chr11:75113400-75118400	Strong transcription	Lung	lung
25	chr11:75113400-75118600	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr11:75113400-75119600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr11:75113400-75120200	Strong transcription	HUES48 Cell Line	embryonic stem cell
28	chr11:75113400-75120200	Strong transcription	Primary B cells from cord blood	blood
29	chr11:75113400-75120200	Strong transcription	Fetal Muscle Trunk	muscle
30	chr11:75113400-75120200	Strong transcription	Sigmoid Colon	Sigmoid Colon
31	chr11:75113600-75117800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:75113600-75118400	Strong transcription	Fetal Kidney	kidney
33	chr11:75113600-75118400	Strong transcription	Placenta Amnion	Placenta Amnion
34	chr11:75113600-75120000	Weak transcription	Right Atrium	heart
35	chr11:75113600-75120200	Strong transcription	H9 Cell Line	embryonic stem cell
36	chr11:75113600-75120200	Strong transcription	Liver	Liver
37	chr11:75113600-75120200	Strong transcription	Fetal Stomach	stomach
38	chr11:75113600-75120200	Strong transcription	Thymus	Thymus
39	chr11:75113600-75120200	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr11:75113800-75117200	Strong transcription	Spleen	Spleen
41	chr11:75113800-75117800	Strong transcription	Colonic Mucosa	Colon
42	chr11:75113800-75118200	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr11:75113800-75118400	Strong transcription	Adipose Nuclei	Adipose
44	chr11:75113800-75118600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:75113800-75119000	Strong transcription	Primary B cells from peripheral blood	blood
46	chr11:75114000-75117600	Genic enhancers	Primary T helper cells PMA-I stimulated	--
47	chr11:75114000-75117600	Genic enhancers	HMEC	breast
48	chr11:75114000-75117800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
49	chr11:75114000-75118400	Strong transcription	Brain Germinal Matrix	brain
50	chr11:75114000-75119200	Strong transcription	Fetal Brain Female	brain

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