Variant report

Variant	nsv555410
Chromosome Location	chr11:72405868-72431679
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:430)
CpG islands
(count:733)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:72416884-72417456	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr11:72416846-72417046	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:72415050-72415061	K562	blood:	n/a	n/a
4	BCL11A	chr11:72430243-72430560	GM12878	blood:	n/a	n/a
5	BCL3	chr11:72427433-72427801	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:72408068-72408270	K562	blood:	n/a	n/a
7	BHLHE40	chr11:72430237-72430443	GM12878	blood:	n/a	n/a
8	BRCA1	chr11:72427687-72427722	GM12878	blood:	n/a	n/a
9	CBX3	chr11:72407961-72408334	K562	blood:	n/a	n/a
10	CCNT2	chr11:72408060-72408768	K562	blood:	n/a	chr11:72408333-72408342 chr11:72408247-72408256
11	CHD2	chr11:72430821-72430887	GM12878	blood:	n/a	n/a
12	CHD2	chr11:72430209-72430531	GM12878	blood:	n/a	n/a
13	CHD2	chr11:72408537-72408570	K562	blood:	n/a	n/a
14	CTBP2	chr11:72416916-72417557	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr11:72415120-72415270	WI-38	lung:	n/a	n/a
16	CTCF	chr11:72415170-72415345	MCF-7	breast:	n/a	n/a
17	CTCF	chr11:72415192-72415315	Gliobla	brain:	n/a	n/a
18	CTCF	chr11:72415160-72415310	A549	lung:	n/a	n/a
19	CTCF	chr11:72415220-72415370	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr11:72415180-72415330	K562	blood:	n/a	n/a
21	CTCF	chr11:72415160-72415310	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr11:72415200-72415350	BJ	skin:	n/a	n/a
23	CTCF	chr11:72414320-72414470	AG04449	skin:	n/a	chr11:72414370-72414379
24	CTCF	chr11:72415200-72415350	AG09319	gingival:	n/a	n/a
25	CTCF	chr11:72415167-72415327	Fibrobl	skin:	n/a	n/a
26	CTCF	chr11:72423260-72423410	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr11:72415209-72415306	GM10266	blood:	n/a	n/a
28	CTCF	chr11:72411280-72411430	HMEC	breast:	n/a	n/a
29	CTCF	chr11:72415195-72415310	GM12878	blood:	n/a	n/a
30	CTCF	chr11:72415060-72415290	GM12864	blood:	n/a	n/a
31	CTCF	chr11:72430752-72430813	GM12892	blood:	n/a	n/a
32	CTCF	chr11:72415220-72415370	AG04449	skin:	n/a	n/a
33	CTCF	chr11:72415200-72415350	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr11:72415260-72415410	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr11:72411288-72411354	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr11:72415220-72415370	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr11:72415173-72415294	ProgFib	skin:	n/a	n/a
38	CTCF	chr11:72415213-72415301	GM12878	blood:	n/a	n/a
39	CTCF	chr11:72415160-72415310	GM12873	blood:	n/a	n/a
40	CTCF	chr11:72415160-72415310	HVMF	connective:	n/a	n/a
41	CTCF	chr11:72415160-72415310	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr11:72415157-72415334	NHEK	skin:	n/a	n/a
43	CTCF	chr11:72414340-72414490	AoAF	blood vessel:	n/a	chr11:72414370-72414379
44	CTCF	chr11:72415161-72415331	HepG2	liver:	n/a	n/a
45	CTCF	chr11:72415120-72415270	HAc	cerebellar:	n/a	n/a
46	CTCF	chr11:72415184-72415331	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:72423240-72423390	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr11:72415200-72415350	HVMF	connective:	n/a	n/a
49	CTCF	chr11:72415120-72415270	HPF	lung:	n/a	n/a
50	CTCF	chr11:72415180-72415330	AG04450	lung:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:72408394-72408444	BE2_C	brain:	n/a
2	chr11:72408394-72408444	BE2_C	brain:	n/a
3	chr11:72408788-72408838	NH-A	brain:	n/a
4	chr11:72407688-72407738	AG09319	gingival:	n/a
5	chr11:72408788-72408838	H1-hESC	embryonic stem cell:	embryo
6	chr11:72408512-72408562	H1-hESC	embryonic stem cell:	embryo
7	chr11:72408394-72408444	GM12891	blood:	n/a
8	chr11:72408394-72408444	GM19239	blood:	n/a
9	chr11:72411400-72411450	A549	lung:	n/a
10	chr11:72408252-72408302	NHBE	bronchial:	n/a
11	chr11:72408252-72408302	HL-60	blood:	n/a
12	chr11:72424620-72424670	GM19239	blood:	n/a
13	chr11:72424441-72424491	Jurkat	blood:	n/a
14	chr11:72408394-72408444	ProgFib	skin:	n/a
15	chr11:72408512-72408562	MCF-7	breast:	n/a
16	chr11:72424620-72424670	GM12878	blood:	n/a
17	chr11:72414453-72414503	GM12891	blood:	n/a
18	chr11:72408252-72408302	BJ	skin:	n/a
19	chr11:72406685-72406735	SK-N-SH_RA	brain:	n/a
20	chr11:72414453-72414503	Jurkat	blood:	n/a
21	chr11:72424441-72424491	HCT-116	colon:	n/a
22	chr11:72424441-72424491	K562	blood:	n/a
23	chr11:72408186-72408236	NB4	blood:	n/a
24	chr11:72408252-72408302	HCF	heart:	n/a
25	chr11:72424620-72424670	T-47D	breast:	n/a
26	chr11:72408788-72408838	A549	lung:	n/a
27	chr11:72406685-72406735	SK-N-SH	brain:	n/a
28	chr11:72414453-72414503	SK-N-MC	brain:	n/a
29	chr11:72408394-72408444	NH-A	brain:	n/a
30	chr11:72408788-72408838	K562	blood:	n/a
31	chr11:72408788-72408838	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:72414453-72414503	HCT-116	colon:	n/a
33	chr11:72424441-72424491	IMR90	lung:	fetal
34	chr11:72408394-72408444	PFSK-1	brain:	n/a
35	chr11:72408186-72408236	HCPEpiC	choroid plexus:	n/a
36	chr11:72417121-72417171	AG09309	skin:	n/a
37	chr11:72424620-72424670	AG04449	skin:	fetal
38	chr11:72411400-72411450	HepG2	liver:	n/a
39	chr11:72408788-72408838	HCPEpiC	choroid plexus:	n/a
40	chr11:72408394-72408444	RPTEC	kidney:	n/a
41	chr11:72408788-72408838	AG04449	skin:	fetal
42	chr11:72417121-72417171	HCM	heart:	n/a
43	chr11:72411400-72411450	HL-60	blood:	n/a
44	chr11:72408394-72408444	HPAEpiC	pulmonary alveolar:	n/a
45	chr11:72424441-72424491	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:72411400-72411450	HCM	heart:	n/a
47	chr11:72424441-72424491	CMK	blood:	n/a
48	chr11:72408788-72408838	HRE	kidney:	n/a
49	chr11:72406685-72406735	PFSK-1	brain:	n/a
50	chr11:72408788-72408838	BJ	skin:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:72427752..72429990-chr11:72433445..72436330,3	MCF-7	breast:
2	chr11:72416171..72418626-chr11:72432345..72434923,2	K562	blood:
3	chr11:72427542..72429481-chr11:72430563..72432228,2	MCF-7	breast:
4	chr11:72430307..72432258-chr11:72433856..72435880,2	MCF-7	breast:
5	chr11:72427542..72429481-chr11:72430563..72432228,2	MCF-7	breast:
6	chr11:72404935..72407742-chr11:72416727..72419484,2	K562	blood:
7	chr11:72429291..72431347-chr11:72435489..72438206,2	K562	blood:
8	chr11:72430803..72433012-chr11:72434377..72436437,3	MCF-7	breast:
9	chr11:72422674..72429269-chr11:72431829..72438308,7	K562	blood:
10	chr11:72407255..72410533-chr11:72414719..72416593,4	K562	blood:
11	chr11:72414882..72417123-chr11:72529003..72531110,2	MCF-7	breast:
12	chr11:72427652..72429994-chr11:72432332..72435084,2	K562	blood:
13	chr11:72406657..72408586-chr11:72553691..72556576,2	MCF-7	breast:
14	chr11:72411342..72413114-chr11:72420679..72423374,2	MCF-7	breast:
15	chr11:72419217..72421589-chr11:72432521..72435426,2	K562	blood:
16	chr11:72408465..72410167-chr11:72410825..72413310,2	K562	blood:
17	chr11:72422011..72424823-chr11:72430319..72431907,2	MCF-7	breast:
18	chr11:72417967..72420999-chr11:72422416..72425990,4	K562	blood:
19	chr11:72415563..72419508-chr11:72423771..72425994,3	K562	blood:
20	chr11:72414757..72417563-chr11:72418152..72422478,6	K562	blood:
21	chr11:72417967..72420999-chr11:72422416..72425990,4	K562	blood:
22	chr11:72407553..72409836-chr11:72411461..72415120,3	MCF-7	breast:
23	chr11:72424924..72427618-chr11:73086077..73088871,2	MCF-7	breast:
24	chr11:72404344..72404880-chr11:72414761..72415395,2	MCF-7	breast:
25	chr11:72407255..72411434-chr11:72413782..72416688,5	K562	blood:
26	chr11:72407255..72411434-chr11:72413782..72416688,5	K562	blood:
27	chr11:72407528..72410167-chr11:72410563..72412325,2	K562	blood:
28	chr11:72404935..72407742-chr11:72416727..72419484,2	K562	blood:
29	chr11:72407528..72410167-chr11:72410563..72412325,2	K562	blood:
30	chr11:72428398..72430412-chr11:72523646..72525946,2	MCF-7	breast:
31	chr11:72415563..72419508-chr11:72423771..72425994,3	K562	blood:
32	chr11:72431679..72434346-chr11:72525248..72526787,2	MCF-7	breast:
33	chr11:72411258..72412804-chr11:72495649..72497466,2	MCF-7	breast:
34	chr11:72411342..72413114-chr11:72420679..72423374,2	MCF-7	breast:
35	chr11:72408052..72410469-chr11:72425945..72427801,2	K562	blood:
36	chr11:72407553..72409836-chr11:72411461..72415120,3	MCF-7	breast:
37	chr11:72406538..72408722-chr11:72523842..72525455,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG16L2-10	chr11:72419231-72419610	NONHSAT022791

No data

Variant related genes	Relation type
ARAP1	TF binding region
ARAP1-AS2	TF binding region
RPS12P20	TF binding region
ARAP1	CpG island
ARAP1-AS2	CpG island
RPS12P20	CpG island
ENSG00000244134	chromatin interactions
ENSG00000168010	chromatin interactions
ENSG00000245148	chromatin interactions
ENSG00000214530	chromatin interactions
ENSG00000054967	chromatin interactions
ENSG00000186635	chromatin interactions
ENSG00000137478	chromatin interactions

Extended variants
information (count: 1182 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1182 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2306608	chr11:72405868-72405869	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs551388516	chr11:72405880-72405881	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569981370	chr11:72405910-72405911	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116784755	chr11:72405914-72405915	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192326695	chr11:72405953-72405954	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs369110604	chr11:72405980-72405981	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs200418570	chr11:72405983-72405984	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs199853378	chr11:72405984-72405985	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183145931	chr11:72405985-72405986	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201049179	chr11:72406006-72406007	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11601039	chr11:72406015-72406016	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544944757	chr11:72406016-72406017	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556682008	chr11:72406029-72406030	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs576715546	chr11:72406040-72406041	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138082807	chr11:72406041-72406042	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs143644813	chr11:72406046-72406047	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs562287909	chr11:72406056-72406057	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs545530995	chr11:72406077-72406078	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376080692	chr11:72406083-72406084	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147580466	chr11:72406086-72406087	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541544829	chr11:72406095-72406096	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs189745190	chr11:72406101-72406102	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs139516775	chr11:72406117-72406118	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200860889	chr11:72406134-72406135	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371143328	chr11:72406149-72406150	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs551793114	chr11:72406187-72406188	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs188055777	chr11:72406190-72406191	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs114988084	chr11:72406201-72406202	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576245671	chr11:72406262-72406263	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs181194864	chr11:72406264-72406265	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs548839262	chr11:72406294-72406295	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs35250343	chr11:72406297-72406298	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs534470584	chr11:72406308-72406309	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113734969	chr11:72406322-72406323	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs552796689	chr11:72406363-72406364	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs374148036	chr11:72406388-72406389	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs376187464	chr11:72406391-72406392	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs370462468	chr11:72406427-72406428	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs149283425	chr11:72406437-72406438	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375239868	chr11:72406494-72406495	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs199904660	chr11:72406495-72406496	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs35361895	chr11:72406505-72406506	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs140387760	chr11:72406525-72406526	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs374344913	chr11:72406550-72406551	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs556952780	chr11:72406561-72406562	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs371492893	chr11:72406563-72406564	Strong transcription Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs550326288	chr11:72406614-72406615	Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs368732834	chr11:72406624-72406625	Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs372334680	chr11:72406646-72406647	Strong transcription Genic enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs376839214	chr11:72406686-72406687	Strong transcription Genic enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Lung cancer	18438408	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
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	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
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72393800-72413400	Strong transcription	Fetal Intestine Small	intestine
2	chr11:72393800-72423200	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr11:72394000-72413800	Strong transcription	Fetal Intestine Large	intestine
4	chr11:72394000-72414600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr11:72394000-72426800	Strong transcription	Thymus	Thymus
6	chr11:72394200-72408000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:72394200-72423600	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr11:72394200-72425800	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr11:72394200-72429000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr11:72394400-72412000	Strong transcription	GM12878-XiMat	blood
11	chr11:72394400-72423200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr11:72394400-72423800	Strong transcription	Duodenum Mucosa	Duodenum
13	chr11:72394400-72424400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr11:72394600-72412800	Strong transcription	Gastric	stomach
15	chr11:72394600-72413200	Strong transcription	Lung	lung
16	chr11:72394600-72428800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:72394600-72429400	Strong transcription	Primary T cells from cord blood	blood
18	chr11:72394600-72430200	Strong transcription	Dnd41	blood
19	chr11:72395000-72408800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr11:72395000-72413600	Strong transcription	Fetal Brain Female	brain
21	chr11:72395000-72423800	Strong transcription	Rectal Mucosa Donor 31	rectum
22	chr11:72395000-72429800	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr11:72395200-72408400	Strong transcription	H9 Cell Line	embryonic stem cell
24	chr11:72395200-72425600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr11:72395200-72429000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr11:72395400-72414200	Strong transcription	Brain Angular Gyrus	brain
27	chr11:72395400-72414200	Strong transcription	Brain Inferior Temporal Lobe	brain
28	chr11:72395400-72414400	Strong transcription	Brain Germinal Matrix	brain
29	chr11:72395800-72414000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr11:72396000-72407800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:72396000-72411000	Strong transcription	NHEK	skin
32	chr11:72396000-72413600	Strong transcription	Brain Cingulate Gyrus	brain
33	chr11:72396000-72413600	Strong transcription	Brain Hippocampus Middle	brain
34	chr11:72396000-72425600	Strong transcription	Primary T helper cells fromperipheralblood	blood
35	chr11:72396000-72426000	Strong transcription	Primary B cells from peripheral blood	blood
36	chr11:72396200-72408400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:72396200-72411000	Strong transcription	HMEC	breast
38	chr11:72396200-72413200	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:72396200-72423200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr11:72396400-72408400	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr11:72396400-72411000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr11:72396400-72425400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr11:72396600-72406600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:72397000-72423400	Strong transcription	Primary B cells from cord blood	blood
45	chr11:72397200-72408800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
46	chr11:72397200-72409800	Strong transcription	Skeletal Muscle Female	skeletal muscle
47	chr11:72397200-72414200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr11:72397400-72414000	Strong transcription	Brain Anterior Caudate	brain
49	chr11:72397800-72410800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr11:72397800-72414000	Strong transcription	Brain Substantia Nigra	brain

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