Variant report

Variant	nsv428573
Chromosome Location	chr11:48032457-48152344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2531)
CpG islands
(count:977)
Chromatin interactive
region (count:136)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:2531 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48082899-48083240	K562	blood:	n/a	n/a
2	ARID3A	chr11:48131445-48131835	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48130891-48131217	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:48095041-48095124	K562	blood:	n/a	n/a
5	ARID3A	chr11:48118839-48119112	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:48114969-48116284	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:48123329-48123998	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:48130883-48131832	K562	blood:	n/a	n/a
9	ARID3A	chr11:48034789-48035164	HepG2	liver:	n/a	n/a
10	ATF1	chr11:48077433-48077920	K562	blood:	n/a	n/a
11	ATF1	chr11:48082834-48083315	K562	blood:	n/a	n/a
12	ATF2	chr11:48077237-48077812	GM12878	blood:	n/a	n/a
13	ATF2	chr11:48131303-48131862	GM12878	blood:	n/a	n/a
14	ATF2	chr11:48040883-48041370	GM12878	blood:	n/a	n/a
15	ATF2	chr11:48128530-48129047	GM12878	blood:	n/a	n/a
16	ATF2	chr11:48041357-48042266	GM12878	blood:	n/a	n/a
17	ATF2	chr11:48053178-48054057	GM12878	blood:	n/a	n/a
18	ATF2	chr11:48041464-48042090	GM12878	blood:	n/a	n/a
19	ATF2	chr11:48040721-48041289	GM12878	blood:	n/a	n/a
20	ATF2	chr11:48125767-48126273	GM12878	blood:	n/a	n/a
21	ATF2	chr11:48085000-48085533	GM12878	blood:	n/a	n/a
22	ATF2	chr11:48073780-48074198	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr11:48034745-48035476	GM12878	blood:	n/a	n/a
24	ATF2	chr11:48040073-48040556	GM12878	blood:	n/a	n/a
25	ATF2	chr11:48125780-48126273	GM12878	blood:	n/a	n/a
26	ATF2	chr11:48131384-48131873	GM12878	blood:	n/a	n/a
27	ATF2	chr11:48128499-48129217	GM12878	blood:	n/a	n/a
28	ATF2	chr11:48094862-48095450	GM12878	blood:	n/a	n/a
29	ATF3	chr11:48082790-48083256	K562	blood:	n/a	n/a
30	ATF3	chr11:48082760-48083237	K562	blood:	n/a	n/a
31	BACH1	chr11:48110331-48110562	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr11:48119683-48119696	K562	blood:	n/a	n/a
33	BACH1	chr11:48082870-48083255	K562	blood:	n/a	n/a
34	BACH1	chr11:48056328-48056343	K562	blood:	n/a	n/a
35	BACH1	chr11:48039773-48040831	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr11:48040138-48040469	GM12878	blood:	n/a	n/a
37	BATF	chr11:48131437-48131740	GM12878	blood:	n/a	n/a
38	BATF	chr11:48041588-48042292	GM12878	blood:	n/a	chr11:48041720-48041728
39	BATF	chr11:48128657-48129110	GM12878	blood:	n/a	n/a
40	BATF	chr11:48085096-48085328	GM12878	blood:	n/a	n/a
41	BATF	chr11:48094903-48095273	GM12878	blood:	n/a	n/a
42	BATF	chr11:48115348-48115634	GM12878	blood:	n/a	n/a
43	BATF	chr11:48131359-48131717	GM12878	blood:	n/a	n/a
44	BATF	chr11:48069274-48069666	GM12878	blood:	n/a	n/a
45	BATF	chr11:48053484-48053871	GM12878	blood:	n/a	chr11:48053699-48053709 chr11:48053698-48053709
46	BATF	chr11:48128651-48129130	GM12878	blood:	n/a	n/a
47	BATF	chr11:48077422-48077763	GM12878	blood:	n/a	n/a
48	BATF	chr11:48041683-48042086	GM12878	blood:	n/a	chr11:48041720-48041728
49	BCL11A	chr11:48131334-48131777	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:48128709-48129015	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48112253-48112303	PFSK-1	brain:	n/a
2	chr11:48112253-48112303	PFSK-1	brain:	n/a
3	chr11:48040772-48040822	MCF-7	breast:	n/a
4	chr11:48057861-48057911	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:48069893-48069943	NH-A	brain:	n/a
6	chr11:48112253-48112303	Caco-2	colon:	n/a
7	chr11:48052092-48052142	AoSMC	blood vessel:	n/a
8	chr11:48065851-48065901	HCM	heart:	n/a
9	chr11:48065851-48065901	Caco-2	colon:	n/a
10	chr11:48112253-48112303	HCPEpiC	choroid plexus:	n/a
11	chr11:48112253-48112303	NH-A	brain:	n/a
12	chr11:48083100-48083150	HEK293	kidney:	embryo
13	chr11:48065851-48065901	BJ	skin:	n/a
14	chr11:48112253-48112303	T-47D	breast:	n/a
15	chr11:48085137-48085187	Hela-S3	cervix:	n/a
16	chr11:48036852-48036902	K562	blood:	n/a
17	chr11:48038449-48038499	HAEpiC	amniotic membrane:	n/a
18	chr11:48038449-48038499	K562	blood:	n/a
19	chr11:48077221-48077271	GM12891	blood:	n/a
20	chr11:48112253-48112303	BJ	skin:	n/a
21	chr11:48085137-48085187	CMK	blood:	n/a
22	chr11:48057861-48057911	HRE	kidney:	n/a
23	chr11:48041783-48041833	AG10803	skin:	n/a
24	chr11:48041783-48041833	GM12891	blood:	n/a
25	chr11:48110045-48110095	BE2_C	brain:	n/a
26	chr11:48034953-48035003	HRPEpiC	eye:	n/a
27	chr11:48065851-48065901	Hela-S3	cervix:	n/a
28	chr11:48129067-48129117	HCM	heart:	n/a
29	chr11:48085137-48085187	NHDF-neo	bronchial:	n/a
30	chr11:48034953-48035003	BJ	skin:	n/a
31	chr11:48040772-48040822	AG09309	skin:	n/a
32	chr11:48118041-48118091	LNCaP	prostate:	n/a
33	chr11:48065851-48065901	PrEC	prostate:	n/a
34	chr11:48057861-48057911	Caco-2	colon:	n/a
35	chr11:48036852-48036902	GM12878	blood:	n/a
36	chr11:48118041-48118091	HCF	heart:	n/a
37	chr11:48034953-48035003	CMK	blood:	n/a
38	chr11:48112253-48112303	GM19239	blood:	n/a
39	chr11:48069893-48069943	HEEpiC	esophagus:	n/a
40	chr11:48112253-48112303	HMEC	breast:	n/a
41	chr11:48040772-48040822	GM12891	blood:	n/a
42	chr11:48041783-48041833	Hela-S3	cervix:	n/a
43	chr11:48034953-48035003	AG09309	skin:	n/a
44	chr11:48041783-48041833	Jurkat	blood:	n/a
45	chr11:48077221-48077271	ECC-1	luminal epithelium:	n/a
46	chr11:48118041-48118091	PANC-1	pancreas:	n/a
47	chr11:48085137-48085187	Caco-2	colon:	n/a
48	chr11:48034953-48035003	HepG2	liver:	n/a
49	chr11:48065851-48065901	SKMC	muscle:	n/a
50	chr11:48038449-48038499	AoSMC	blood vessel:	n/a

(count:136 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
2	chr11:48061733..48064075-chr11:48066877..48069020,2	K562	blood:
3	chr11:48087146..48090054-chr11:48094817..48096585,2	MCF-7	breast:
4	chr11:48082980..48084917-chr11:48096551..48099093,2	K562	blood:
5	chr11:48047876..48049953-chr11:48109269..48111434,2	MCF-7	breast:
6	chr11:48120614..48123449-chr11:48129423..48131714,2	MCF-7	breast:
7	chr11:48142980..48145287-chr11:48148448..48150580,3	MCF-7	breast:
8	chr11:48081883..48084532-chr11:48088077..48090811,2	MCF-7	breast:
9	chr11:48046572..48047306-chr11:48130972..48131586,2	MCF-7	breast:
10	chr11:48073485..48075927-chr11:48082055..48084574,2	MCF-7	breast:
11	chr11:48121014..48122957-chr11:48124539..48127155,2	K562	blood:
12	chr11:48047876..48049953-chr11:48109269..48111434,2	MCF-7	breast:
13	chr11:47985506..47986348-chr11:48130588..48131464,3	MCF-7	breast:
14	chr11:48069835..48071887-chr11:48083817..48085807,2	MCF-7	breast:
15	chr11:48001502..48002444-chr11:48131229..48132098,2	MCF-7	breast:
16	chr11:48098800..48100999-chr11:48104120..48106582,2	MCF-7	breast:
17	chr11:48051913..48054330-chr11:48054555..48057402,3	MCF-7	breast:
18	chr11:48086913..48088924-chr11:48093954..48095544,2	K562	blood:
19	chr11:48037574..48039959-chr11:48041081..48044491,3	K562	blood:
20	chr11:48112031..48113821-chr11:48114417..48116008,2	K562	blood:
21	chr11:48001276..48003972-chr11:48068984..48071526,3	MCF-7	breast:
22	chr11:48035360..48038062-chr11:48039286..48041376,2	MCF-7	breast:
23	chr11:48072169..48075662-chr11:48075736..48079290,4	MCF-7	breast:
24	chr11:48035577..48038589-chr11:48041856..48045572,3	MCF-7	breast:
25	chr11:48068334..48069860-chr11:48070016..48072544,2	MCF-7	breast:
26	chr11:48105031..48106761-chr11:48108023..48109885,2	MCF-7	breast:
27	chr11:48061951..48065074-chr11:48065733..48069871,4	MCF-7	breast:
28	chr11:48119543..48121197-chr11:48126844..48128670,2	K562	blood:
29	chr11:48031281..48033125-chr11:48036287..48038238,2	MCF-7	breast:
30	chr11:48011467..48013224-chr11:48076838..48078616,2	K562	blood:
31	chr11:48082980..48084917-chr11:48096551..48099093,2	K562	blood:
32	chr11:48077913..48080280-chr11:48080886..48083753,2	K562	blood:
33	chr11:47967015..47968589-chr11:48075080..48077424,2	MCF-7	breast:
34	chr11:48129232..48130878-chr11:48134176..48136053,2	K562	blood:
35	chr11:48024330..48026388-chr11:48082917..48084428,2	K562	blood:
36	chr11:48015448..48018346-chr11:48050967..48053426,2	MCF-7	breast:
37	chr11:48109181..48111732-chr11:48113222..48115393,2	K562	blood:
38	chr11:48107721..48110377-chr11:48121800..48123863,2	MCF-7	breast:
39	chr11:47985574..47986089-chr11:48131663..48132191,2	K562	blood:
40	chr11:47955472..47956729-chr11:48130954..48132546,8	MCF-7	breast:
41	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
42	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
43	chr11:48125100..48126917-chr11:48129444..48131504,2	MCF-7	breast:
44	chr11:47955523..47956710-chr11:48130209..48132188,17	MCF-7	breast:
45	chr11:48081533..48083185-chr11:48091579..48093994,2	MCF-7	breast:
46	chr11:47879130..47879931-chr11:48131064..48131706,2	MCF-7	breast:
47	chr11:48071848..48074782-chr11:48077801..48079441,2	MCF-7	breast:
48	chr11:48077913..48080280-chr11:48080886..48083753,2	K562	blood:
49	chr11:48063050..48065981-chr11:48070901..48073953,3	MCF-7	breast:
50	chr11:18993520..18994020-chr11:48120012..48120966,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP160-1	chr11:48035958-48036229	ENSG00000254879.1
2	lnc-NUP160-1	chr11:48037379-48037407	ENSG00000254879.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3161	chr11:48118343-48118365	MIMAT0015035

No data

Variant related genes	Relation type
PTPRJ	TF binding region
MIR3161	TF binding region
ENSG00000254879	TF binding region
PTPRJ	CpG island
MIR3161	CpG island
ENSG00000254879	CpG island
ENSG00000030066	chromatin interactions
ENSG00000149177	chromatin interactions
ENSG00000254879	chromatin interactions
ENSG00000165923	chromatin interactions

Extended variants
information (count: 4151 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4151 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144390514	chr11:48032478-48032479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs553329411	chr11:48032487-48032488	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557362094	chr11:48032489-48032490	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528000967	chr11:48032506-48032507	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs556630879	chr11:48032514-48032515	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1228033	chr11:48032521-48032522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs112461155	chr11:48032527-48032528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs140182323	chr11:48032658-48032659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142435071	chr11:48032663-48032664	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572596719	chr11:48032667-48032668	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs193280085	chr11:48032733-48032734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs151251716	chr11:48032775-48032776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564495228	chr11:48032788-48032789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs117633933	chr11:48032800-48032801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546028606	chr11:48032815-48032816	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs200366207	chr11:48032837-48032838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs567216050	chr11:48032940-48032941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562648187	chr11:48032990-48032991	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184252876	chr11:48032998-48032999	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs550286215	chr11:48033053-48033054	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs140430408	chr11:48033196-48033197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570033062	chr11:48033275-48033276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567941453	chr11:48033282-48033283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189509659	chr11:48033286-48033287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs35396880	chr11:48033302-48033303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547130646	chr11:48033364-48033365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532914537	chr11:48033389-48033390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538081498	chr11:48033414-48033415	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs77207953	chr11:48033420-48033421	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs539065703	chr11:48033433-48033434	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs556776988	chr11:48033434-48033435	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs150435992	chr11:48033582-48033583	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs181167152	chr11:48033583-48033584	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs555977566	chr11:48033593-48033594	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs572715786	chr11:48033599-48033600	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs79560246	chr11:48033664-48033665	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs558284636	chr11:48033684-48033685	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs577926031	chr11:48033714-48033715	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs543466452	chr11:48033805-48033806	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs185471238	chr11:48033835-48033836	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs531484721	chr11:48033903-48033904	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs11601764	chr11:48033919-48033920	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs561536722	chr11:48033933-48033934	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs569150926	chr11:48033942-48033943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs76607067	chr11:48033971-48033972	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs547044207	chr11:48033986-48033987	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs147691879	chr11:48034053-48034054	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs188792761	chr11:48034054-48034055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs72899723	chr11:48034131-48034132	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs181539438	chr11:48034141-48034142	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Glioblastoma multiforme	21390271	CNVD
Acute lymphoblastic leukemia	20699438	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21990379	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:5150 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48018800-48042000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr11:48025000-48045200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:48026000-48039200	Weak transcription	Fetal Kidney	kidney
4	chr11:48026400-48039200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:48027400-48037600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr11:48027400-48044000	Enhancers	Primary T cells fromperipheralblood	blood
7	chr11:48027600-48034800	Weak transcription	Small Intestine	intestine
8	chr11:48027800-48037600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr11:48027800-48037800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr11:48027800-48039000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr11:48028000-48032800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr11:48028000-48034000	Weak transcription	Fetal Intestine Large	intestine
13	chr11:48028000-48034200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr11:48028000-48034600	Weak transcription	Fetal Intestine Small	intestine
15	chr11:48028000-48038800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr11:48028200-48033800	Weak transcription	Placenta	Placenta
17	chr11:48028200-48034000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr11:48028200-48034800	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr11:48028400-48032600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr11:48028400-48032800	Weak transcription	Gastric	stomach
21	chr11:48028400-48033400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr11:48028400-48034000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:48028400-48034800	Weak transcription	Brain Angular Gyrus	brain
24	chr11:48028400-48034800	Weak transcription	Fetal Muscle Leg	muscle
25	chr11:48028400-48034800	Weak transcription	Right Atrium	heart
26	chr11:48028400-48038800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr11:48028400-48039200	Weak transcription	Fetal Stomach	stomach
28	chr11:48028600-48032600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:48028600-48032600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr11:48028600-48033600	Weak transcription	Brain Anterior Caudate	brain
31	chr11:48028600-48033600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr11:48028600-48033600	Weak transcription	Fetal Heart	heart
33	chr11:48028600-48033800	Weak transcription	NH-A	brain
34	chr11:48028600-48034800	Weak transcription	Colon Smooth Muscle	Colon
35	chr11:48028600-48035200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr11:48028600-48035600	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr11:48029400-48032800	Weak transcription	Primary T cells from cord blood	blood
38	chr11:48029400-48033800	Weak transcription	Brain Substantia Nigra	brain
39	chr11:48029400-48034000	Weak transcription	Duodenum Mucosa	Duodenum
40	chr11:48029400-48034600	Weak transcription	Stomach Mucosa	stomach
41	chr11:48029400-48034800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr11:48029600-48032800	Weak transcription	Brain Hippocampus Middle	brain
43	chr11:48029600-48033600	Weak transcription	Left Ventricle	heart
44	chr11:48029600-48033800	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr11:48029600-48034000	Weak transcription	NHDF-Ad	bronchial
46	chr11:48029600-48034600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr11:48029600-48034600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr11:48029600-48034600	Weak transcription	NHLF	lung
49	chr11:48029600-48034800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:48029600-48034800	Weak transcription	Adipose Nuclei	Adipose

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