Variant report

Variant	esv34768
Chromosome Location	chr11:121452651-121534938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1880)
CpG islands
(count:1163)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1880 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:121525601-121525850	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:121526244-121527300	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:121456665-121456680	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:121462057-121462420	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:121532722-121532870	HepG2	liver:	n/a	n/a
6	ATF1	chr11:121462166-121462512	K562	blood:	n/a	n/a
7	ATF2	chr11:121460309-121461845	GM12878	blood:	n/a	n/a
8	ATF2	chr11:121463338-121463847	GM12878	blood:	n/a	n/a
9	ATF2	chr11:121460260-121461812	GM12878	blood:	n/a	n/a
10	ATF2	chr11:121461996-121462649	GM12878	blood:	n/a	n/a
11	ATF2	chr11:121463443-121463810	GM12878	blood:	n/a	n/a
12	BACH1	chr11:121525996-121526967	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr11:121460641-121461440	GM12878	blood:	n/a	chr11:121461005-121461016
14	BATF	chr11:121463446-121463715	GM12878	blood:	n/a	n/a
15	BATF	chr11:121460536-121461472	GM12878	blood:	n/a	chr11:121461005-121461016
16	BATF	chr11:121463471-121463715	GM12878	blood:	n/a	n/a
17	BCL11A	chr11:121460541-121461528	GM12878	blood:	n/a	n/a
18	BCL11A	chr11:121460569-121461315	GM12878	blood:	n/a	n/a
19	BCL3	chr11:121505572-121505937	GM12878	blood:	n/a	n/a
20	BCL3	chr11:121460476-121461344	GM12878	blood:	n/a	n/a
21	BCL3	chr11:121460618-121461380	GM12878	blood:	n/a	n/a
22	BCLAF1	chr11:121460517-121461846	GM12878	blood:	n/a	n/a
23	BCLAF1	chr11:121462089-121462535	GM12878	blood:	n/a	n/a
24	BCLAF1	chr11:121461910-121462508	GM12878	blood:	n/a	n/a
25	BCLAF1	chr11:121460453-121461855	GM12878	blood:	n/a	n/a
26	BHLHE40	chr11:121460369-121461611	GM12878	blood:	n/a	n/a
27	BHLHE40	chr11:121526219-121527120	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:121466496-121466728	A549	lung:	n/a	n/a
29	BHLHE40	chr11:121526179-121527010	K562	blood:	n/a	n/a
30	BHLHE40	chr11:121526190-121527541	HepG2	liver:	n/a	n/a
31	BHLHE40	chr11:121462175-121462424	K562	blood:	n/a	n/a
32	BHLHE40	chr11:121462129-121462470	GM12878	blood:	n/a	n/a
33	BRCA1	chr11:121526207-121526407	HepG2	liver:	n/a	n/a
34	BRCA1	chr11:121526704-121526980	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr11:121526282-121527099	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr11:121526642-121526987	K562	blood:	n/a	n/a
37	CCNT2	chr11:121526746-121527053	K562	blood:	n/a	n/a
38	CEBPB	chr11:121466403-121466792	MCF-7	breast:	n/a	n/a
39	CEBPB	chr11:121466388-121466905	MCF-7	breast:	n/a	n/a
40	CEBPB	chr11:121507459-121507768	ECC-1	luminal epithelium:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
41	CEBPB	chr11:121526243-121527132	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:121504169-121504450	IMR90	lung:	n/a	n/a
43	CEBPB	chr11:121505335-121505941	IMR90	lung:	n/a	chr11:121505621-121505632
44	CEBPB	chr11:121507662-121507700	K562	blood:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
45	CEBPB	chr11:121526125-121527177	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:121466449-121466737	HepG2	liver:	n/a	n/a
47	CEBPB	chr11:121466364-121467020	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr11:121507532-121507823	Hela-S3	cervix:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
49	CEBPB	chr11:121507500-121507859	A549	lung:	n/a	chr11:121507681-121507692 chr11:121507683-121507692 chr11:121507683-121507692
50	CEBPB	chr11:121505487-121505767	K562	blood:	n/a	chr11:121505621-121505632

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:121524538-121524588	BE2_C	brain:	n/a
2	chr11:121526840-121526890	AG04450	lung:	fetal
3	chr11:121466463-121466513	NHBE	bronchial:	n/a
4	chr11:121515019-121515069	K562	blood:	n/a
5	chr11:121524538-121524588	BE2_C	brain:	n/a
6	chr11:121526840-121526890	AG04450	lung:	fetal
7	chr11:121466463-121466513	NHBE	bronchial:	n/a
8	chr11:121515019-121515069	K562	blood:	n/a
9	chr11:121474197-121474247	U87	brain:	n/a
10	chr11:121533431-121533481	HMEC	breast:	n/a
11	chr11:121466463-121466513	HCM	heart:	n/a
12	chr11:121507724-121507774	Caco-2	colon:	n/a
13	chr11:121526609-121526659	HRPEpiC	eye:	n/a
14	chr11:121502395-121502445	RPTEC	kidney:	n/a
15	chr11:121515019-121515069	AG04449	skin:	fetal
16	chr11:121474197-121474247	LNCaP	prostate:	n/a
17	chr11:121477737-121477787	AoSMC	blood vessel:	n/a
18	chr11:121526840-121526890	SAEC	small airway:	n/a
19	chr11:121466430-121466480	NHDF-neo	bronchial:	n/a
20	chr11:121466629-121466679	HRPEpiC	eye:	n/a
21	chr11:121466463-121466513	AG04450	lung:	fetal
22	chr11:121477737-121477787	A549	lung:	n/a
23	chr11:121460778-121460828	HEK293	kidney:	embryo
24	chr11:121533431-121533481	LNCaP	prostate:	n/a
25	chr11:121466430-121466480	PANC-1	pancreas:	n/a
26	chr11:121477737-121477787	GM19239	blood:	n/a
27	chr11:121526609-121526659	GM12892	blood:	n/a
28	chr11:121466629-121466679	ECC-1	luminal epithelium:	n/a
29	chr11:121474197-121474247	AG04449	skin:	fetal
30	chr11:121477737-121477787	AG04450	lung:	fetal
31	chr11:121526609-121526659	HEEpiC	esophagus:	n/a
32	chr11:121502395-121502445	H1-hESC	embryonic stem cell:	embryo
33	chr11:121507724-121507774	SAEC	small airway:	n/a
34	chr11:121460778-121460828	PrEC	prostate:	n/a
35	chr11:121524538-121524588	HCM	heart:	n/a
36	chr11:121477655-121477705	MCF10A-Er-Src	breast:	n/a
37	chr11:121460778-121460828	CMK	blood:	n/a
38	chr11:121466430-121466480	SK-N-SH_RA	brain:	n/a
39	chr11:121502395-121502445	HNPCEpiC	eye:	n/a
40	chr11:121507724-121507774	T-47D	breast:	n/a
41	chr11:121524538-121524588	SK-N-SH_RA	brain:	n/a
42	chr11:121519649-121519699	GM12892	blood:	n/a
43	chr11:121533431-121533481	SK-N-SH	brain:	n/a
44	chr11:121477655-121477705	BE2_C	brain:	n/a
45	chr11:121515019-121515069	T-47D	breast:	n/a
46	chr11:121477655-121477705	AG09309	skin:	n/a
47	chr11:121466430-121466480	IMR90	lung:	fetal
48	chr11:121519649-121519699	HEK293	kidney:	embryo
49	chr11:121474197-121474247	SAEC	small airway:	n/a
50	chr11:121526840-121526890	PANC-1	pancreas:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:121515868..121518433-chr11:121526478..121527992,2	K562	blood:
2	chr11:121524308..121528407-chr11:121529156..121532838,3	K562	blood:
3	chr11:121526110..121526861-chr11:122376172..122377002,2	K562	blood:
4	chr11:121512816..121514316-chr17:41399595..41402548,2	MCF-7	breast:
5	chr11:121192033..121192612-chr11:121461567..121462290,2	MCF-7	breast:
6	chr11:121515868..121518433-chr11:121526478..121527992,2	K562	blood:
7	chr11:121189831..121190442-chr11:121461888..121462730,2	MCF-7	breast:
8	chr11:121316893..121318248-chr11:121461711..121462415,3	MCF-7	breast:
9	chr11:121526442..121527320-chr11:122376172..122377075,6	MCF-7	breast:
10	chr11:121525946..121527352-chr11:122073329..122074247,11	MCF-7	breast:
11	chr11:121488832..121492923-chr11:121494735..121499119,4	K562	blood:
12	chr11:121492728..121494563-chr11:121521550..121524030,2	K562	blood:
13	chr11:120381894..120382837-chr11:121461399..121462390,3	K562	blood:
14	chr11:121526799..121527341-chr11:122073257..122073852,3	K562	blood:
15	chr11:121526136..121527320-chr11:122073409..122074417,3	MCF-7	breast:
16	chr11:120975216..120977193-chr11:121456635..121459591,2	K562	blood:
17	chr11:121192094..121192920-chr11:121461877..121462689,3	MCF-7	breast:
18	chr11:121492728..121494563-chr11:121521550..121524030,2	K562	blood:
19	chr11:121524308..121528407-chr11:121529156..121532838,3	K562	blood:
20	chr11:121525458..121528227-chr11:122072456..122075011,2	MCF-7	breast:
21	chr11:121512836..121514336-chr17:41466392..41468507,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BLID-6	chr11:121471818-121474271	ucscGeneNc_uc001pye_1
2	lnc-BLID-7	chr11:121476292-121476369	ucscGeneNc_uc001pya_2
3	lnc-BLID-7	chr11:121465023-121467658	ucscGeneNc_uc001pya_2

No data

Variant related genes	Relation type
SORL1	TF binding region
SORL1	CpG island
ENSG00000255090	chromatin interactions
ENSG00000204306	chromatin interactions
ENSG00000149403	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000137642	chromatin interactions

Extended variants
information (count: 3202 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3202 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11218350	chr11:121452651-121452652	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183109634	chr11:121452681-121452682	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs556823759	chr11:121452686-121452687	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs150694907	chr11:121452702-121452703	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs542061850	chr11:121452708-121452709	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs139934548	chr11:121452739-121452740	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs572243155	chr11:121452854-121452855	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs143186982	chr11:121452900-121452901	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs564398701	chr11:121452910-121452911	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs570920264	chr11:121452926-121452927	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs538248424	chr11:121452958-121452959	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs76994404	chr11:121453022-121453023	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs549868555	chr11:121453025-121453026	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs375992301	chr11:121453066-121453067	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs80217871	chr11:121453067-121453068	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs140304886	chr11:121453111-121453112	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs186770011	chr11:121453136-121453137	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs566688592	chr11:121453161-121453162	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs191725950	chr11:121453171-121453172	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs144041719	chr11:121453226-121453227	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs552251863	chr11:121453229-121453230	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs183450417	chr11:121453232-121453233	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs537886528	chr11:121453303-121453304	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs555880098	chr11:121453310-121453311	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs11604875	chr11:121453338-121453339	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568754566	chr11:121453346-121453347	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs145030556	chr11:121453360-121453361	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs535733584	chr11:121453454-121453455	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs554012569	chr11:121453474-121453475	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs12292354	chr11:121453492-121453493	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs3781838	chr11:121453517-121453518	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs74412989	chr11:121453519-121453520	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs576451840	chr11:121453527-121453528	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs543846530	chr11:121453572-121453573	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs149088597	chr11:121453593-121453594	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs529268912	chr11:121453633-121453634	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs548524111	chr11:121453663-121453664	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs558232310	chr11:121453703-121453704	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs11218351	chr11:121453707-121453708	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs527490732	chr11:121453720-121453721	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs58698151	chr11:121453779-121453780	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs76490923	chr11:121453783-121453784	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs537520344	chr11:121453831-121453832	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs549779483	chr11:121453873-121453874	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs11218352	chr11:121453898-121453899	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs535057110	chr11:121453922-121453923	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs554049325	chr11:121453923-121453924	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs143106968	chr11:121453931-121453932	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs540066095	chr11:121453975-121453976	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs187840309	chr11:121453986-121453987	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Squamous cell cancer	20885788	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21385341	CNVD
Multiple myeloma	16461302	CNVD
Burkitt''s lymphoma	18698080	CNVD
Prostate cancer	23792589	CNVD
Effusion lymphoma	18079361	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:2148 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121407200-121459000	Weak transcription	Colon Smooth Muscle	Colon
2	chr11:121416600-121471800	Strong transcription	Primary T cells from cord blood	blood
3	chr11:121425000-121456800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr11:121431000-121466400	Weak transcription	Ovary	ovary
5	chr11:121434600-121453200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr11:121435200-121464800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr11:121437800-121453600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr11:121438400-121453600	Weak transcription	Colonic Mucosa	Colon
9	chr11:121440600-121485000	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr11:121442200-121456800	Weak transcription	Esophagus	oesophagus
11	chr11:121443000-121455000	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr11:121443400-121464600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr11:121443800-121456800	Weak transcription	Lung	lung
14	chr11:121443800-121458600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr11:121443800-121461600	Weak transcription	Pancreas	Pancrea
16	chr11:121445000-121454600	Strong transcription	Fetal Intestine Large	intestine
17	chr11:121446800-121453200	Weak transcription	Right Atrium	heart
18	chr11:121448200-121453600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr11:121448200-121453600	Weak transcription	Spleen	Spleen
20	chr11:121448400-121461200	Weak transcription	Gastric	stomach
21	chr11:121448800-121495600	Weak transcription	Stomach Mucosa	stomach
22	chr11:121449600-121457200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr11:121449800-121465800	Weak transcription	Adipose Nuclei	Adipose
24	chr11:121450000-121453000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr11:121450000-121460200	Weak transcription	Brain Germinal Matrix	brain
26	chr11:121450200-121453000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr11:121450200-121453600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr11:121450200-121453800	Weak transcription	Aorta	Aorta
29	chr11:121450200-121453800	Weak transcription	HMEC	breast
30	chr11:121450200-121455200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr11:121450200-121456400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr11:121450200-121458600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr11:121450200-121460800	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr11:121450200-121461600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr11:121450200-121461800	Weak transcription	Fetal Brain Male	brain
36	chr11:121450400-121453200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr11:121450600-121460600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:121451000-121453600	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr11:121451000-121453600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr11:121451000-121457800	Weak transcription	Fetal Lung	lung
41	chr11:121451000-121462600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr11:121451200-121452800	Enhancers	Dnd41	blood
43	chr11:121451200-121453400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr11:121451200-121454200	Enhancers	Primary hematopoietic stem cells	blood
45	chr11:121451200-121455600	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr11:121451200-121456800	Weak transcription	Fetal Brain Female	brain
47	chr11:121451200-121461600	Weak transcription	Fetal Kidney	kidney
48	chr11:121451200-121464000	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr11:121451200-121488200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
50	chr11:121451400-121453600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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