Variant report

Variant	nsv897649
Chromosome Location	chr11:63761169-63844683
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2009)
CpG islands
(count:3849)
Chromatin interactive
region (count:159)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2009 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:63775279-63775620	K562	blood:	n/a	n/a
2	ARID3A	chr11:63775280-63775601	HepG2	liver:	n/a	n/a
3	ATF1	chr11:63775311-63775619	K562	blood:	n/a	n/a
4	ATF2	chr11:63765834-63766357	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr11:63767064-63767328	GM12878	blood:	n/a	n/a
6	ATF2	chr11:63766903-63767235	GM12878	blood:	n/a	n/a
7	ATF2	chr11:63792675-63792990	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr11:63772005-63772436	K562	blood:	n/a	n/a
9	ATF3	chr11:63770902-63771103	K562	blood:	n/a	chr11:63771039-63771053
10	ATF3	chr11:63841753-63841975	K562	blood:	n/a	n/a
11	BACH1	chr11:63767436-63767607	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:63775210-63775560	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:63775343-63775555	K562	blood:	n/a	n/a
14	BACH1	chr11:63774825-63775008	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr11:63791417-63791759	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr11:63802876-63802981	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:63766437-63767186	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr11:63764721-63765243	K562	blood:	n/a	n/a
19	BCL3	chr11:63765401-63766255	K562	blood:	n/a	n/a
20	BCL3	chr11:63774182-63775698	A549	lung:	n/a	chr11:63774220-63774233
21	BCL3	chr11:63768826-63769206	A549	lung:	n/a	n/a
22	BCL3	chr11:63774489-63775789	A549	lung:	n/a	n/a
23	BCLAF1	chr11:63775214-63775699	K562	blood:	n/a	n/a
24	BCLAF1	chr11:63767874-63768219	GM12878	blood:	n/a	chr11:63767947-63767960 chr11:63767943-63767956 chr11:63767949-63767962 chr11:63767950-63767963 chr11:63768128-63768141
25	BHLHE40	chr11:63775269-63775558	HepG2	liver:	n/a	chr11:63775436-63775452
26	BHLHE40	chr11:63841798-63842043	K562	blood:	n/a	n/a
27	BHLHE40	chr11:63775246-63775565	A549	lung:	n/a	chr11:63775436-63775452
28	BHLHE40	chr11:63804009-63804180	K562	blood:	n/a	n/a
29	BHLHE40	chr11:63768018-63768154	GM12878	blood:	n/a	chr11:63768053-63768069
30	BHLHE40	chr11:63774514-63774932	K562	blood:	n/a	n/a
31	BHLHE40	chr11:63789158-63789396	K562	blood:	n/a	n/a
32	BHLHE40	chr11:63815684-63815903	HepG2	liver:	n/a	n/a
33	BHLHE40	chr11:63775133-63775706	K562	blood:	n/a	chr11:63775436-63775452
34	BHLHE40	chr11:63775381-63775479	GM12878	blood:	n/a	chr11:63775436-63775452
35	BHLHE40	chr11:63789157-63789357	HepG2	liver:	n/a	n/a
36	BHLHE40	chr11:63775075-63775633	HepG2	liver:	n/a	chr11:63775436-63775452
37	BRCA1	chr11:63775214-63775325	HepG2	liver:	n/a	n/a
38	BRCA1	chr11:63815522-63815611	HepG2	liver:	n/a	n/a
39	CBX3	chr11:63775189-63775636	K562	blood:	n/a	n/a
40	CBX3	chr11:63772036-63772445	K562	blood:	n/a	n/a
41	CBX3	chr11:63807405-63807674	K562	blood:	n/a	n/a
42	CBX3	chr11:63775300-63775534	K562	blood:	n/a	n/a
43	CCNT2	chr11:63768203-63768343	K562	blood:	n/a	n/a
44	CCNT2	chr11:63828186-63828923	K562	blood:	n/a	chr11:63828358-63828367
45	CCNT2	chr11:63767134-63767334	K562	blood:	n/a	n/a
46	CCNT2	chr11:63775082-63775801	K562	blood:	n/a	chr11:63775179-63775188
47	CCNT2	chr11:63796085-63796179	K562	blood:	n/a	chr11:63796120-63796129 chr11:63796152-63796161
48	CCNT2	chr11:63766172-63766838	K562	blood:	n/a	n/a
49	CEBPB	chr11:63762605-63762787	K562	blood:	n/a	n/a
50	CEBPB	chr11:63802448-63802686	HepG2	liver:	n/a	chr11:63802588-63802599

(count:3849 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:63784126-63784176	BJ	skin:	n/a
2	chr11:63802973-63803023	AoSMC	blood vessel:	n/a
3	chr11:63767176-63767226	PrEC	prostate:	n/a
4	chr11:63766546-63766596	SK-N-SH	brain:	n/a
5	chr11:63766787-63766837	GM06990	blood:	n/a
6	chr11:63767561-63767611	Hepatocyte	liver:	n/a
7	chr11:63784126-63784176	BJ	skin:	n/a
8	chr11:63802973-63803023	AoSMC	blood vessel:	n/a
9	chr11:63767176-63767226	PrEC	prostate:	n/a
10	chr11:63766546-63766596	SK-N-SH	brain:	n/a
11	chr11:63766787-63766837	GM06990	blood:	n/a
12	chr11:63767561-63767611	Hepatocyte	liver:	n/a
13	chr11:63772824-63772874	HL-60	blood:	n/a
14	chr11:63775226-63775276	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:63764217-63764267	BE2_C	brain:	n/a
16	chr11:63804044-63804094	AG04450	lung:	fetal
17	chr11:63784126-63784176	RPTEC	kidney:	n/a
18	chr11:63768665-63768715	AG09319	gingival:	n/a
19	chr11:63789520-63789570	T-47D	breast:	n/a
20	chr11:63839479-63839529	K562	blood:	n/a
21	chr11:63796982-63797032	AG04449	skin:	fetal
22	chr11:63766286-63766336	GM12891	blood:	n/a
23	chr11:63766286-63766336	PrEC	prostate:	n/a
24	chr11:63764804-63764854	MCF-7	breast:	n/a
25	chr11:63804021-63804071	SK-N-MC	brain:	n/a
26	chr11:63764804-63764854	LNCaP	prostate:	n/a
27	chr11:63828762-63828812	HNPCEpiC	eye:	n/a
28	chr11:63772824-63772874	HCF	heart:	n/a
29	chr11:63765561-63765611	HAEpiC	amniotic membrane:	n/a
30	chr11:63767176-63767226	Hela-S3	cervix:	n/a
31	chr11:63775436-63775486	H1-hESC	embryonic stem cell:	embryo
32	chr11:63828039-63828089	U87	brain:	n/a
33	chr11:63767176-63767226	GM19239	blood:	n/a
34	chr11:63768032-63768082	ECC-1	luminal epithelium:	n/a
35	chr11:63768032-63768082	Jurkat	blood:	n/a
36	chr11:63839511-63839561	HCPEpiC	choroid plexus:	n/a
37	chr11:63768412-63768462	U87	brain:	n/a
38	chr11:63768665-63768715	HRCEpiC	kidney:	n/a
39	chr11:63799985-63800035	HepG2	liver:	n/a
40	chr11:63804021-63804071	GM12892	blood:	n/a
41	chr11:63803845-63803895	PFSK-1	brain:	n/a
42	chr11:63784126-63784176	AG04449	skin:	fetal
43	chr11:63775226-63775276	HRPEpiC	eye:	n/a
44	chr11:63768665-63768715	NHBE	bronchial:	n/a
45	chr11:63768040-63768090	NHDF-neo	bronchial:	n/a
46	chr11:63767561-63767611	HepG2	liver:	n/a
47	chr11:63784102-63784152	AG10803	skin:	n/a
48	chr11:63804119-63804169	AG09319	gingival:	n/a
49	chr11:63803781-63803831	GM06990	blood:	n/a
50	chr11:63803781-63803831	CMK	blood:	n/a

(count:159 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:63794408..63798675-chr11:63803501..63805972,4	MCF-7	breast:
2	chr11:63753869..63755637-chr11:63777249..63778966,2	MCF-7	breast:
3	chr11:63753248..63755186-chr11:63788577..63790705,2	MCF-7	breast:
4	chr11:63783548..63786701-chr11:63788773..63791378,4	K562	blood:
5	chr11:63819451..63820983-chr11:63825427..63828191,2	MCF-7	breast:
6	chr11:63822085..63823852-chr11:63832946..63834893,2	K562	blood:
7	chr11:63775790..63777703-chr11:63802997..63805194,2	K562	blood:
8	chr11:63763212..63764799-chr11:63914863..63917321,2	MCF-7	breast:
9	chr11:63770570..63773392-chr11:63780661..63782649,3	K562	blood:
10	chr11:63779470..63782792-chr11:63782839..63786863,3	K562	blood:
11	chr11:63811316..63814107-chr11:63816433..63819262,2	K562	blood:
12	chr11:63751963..63753694-chr11:63759818..63761321,2	K562	blood:
13	chr11:63807919..63809240-chr11:63915893..63916601,3	MCF-7	breast:
14	chr11:63806792..63809635-chr11:63899268..63901371,2	K562	blood:
15	chr11:63774815..63776528-chr11:63778908..63781240,2	K562	blood:
16	chr11:63797239..63799107-chr11:63825801..63827534,2	K562	blood:
17	chr11:63788278..63790880-chr11:63809283..63811102,2	MCF-7	breast:
18	chr11:63790185..63792388-chr11:63795065..63797740,2	K562	blood:
19	chr11:63805907..63808645-chr11:63818618..63820814,2	MCF-7	breast:
20	chr11:63785398..63788201-chr11:63813815..63816275,2	K562	blood:
21	chr11:63815764..63818216-chr11:63818640..63821960,4	K562	blood:
22	chr11:63811316..63814107-chr11:63816433..63819262,2	K562	blood:
23	chr11:63767743..63768450-chr16:50186380..50187229,2	NB4	blood:
24	chr11:63788062..63790678-chr11:63896459..63899438,2	K562	blood:
25	chr11:63608184..63610790-chr11:63772494..63774086,2	K562	blood:
26	chr11:63752288..63756029-chr11:63763681..63768717,11	MCF-7	breast:
27	chr11:63783940..63785557-chr11:63787876..63789715,2	MCF-7	breast:
28	chr11:63786154..63788188-chr11:63951633..63953314,2	MCF-7	breast:
29	chr11:63784023..63786647-chr11:64006820..64008419,2	K562	blood:
30	chr11:63785398..63788201-chr11:63813815..63816275,2	K562	blood:
31	chr11:63807602..63810051-chr11:63813403..63816265,2	MCF-7	breast:
32	chr11:63833676..63835809-chr11:63838018..63839588,2	MCF-7	breast:
33	chr11:63793092..63798185-chr11:63799331..63804934,6	K562	blood:
34	chr11:63803039..63805403-chr11:63810325..63812518,2	K562	blood:
35	chr11:63827427..63831095-chr11:63832990..63836351,3	K562	blood:
36	chr11:63783548..63786701-chr11:63788773..63791378,4	K562	blood:
37	chr11:63806637..63808238-chr11:64215828..64217330,2	MCF-7	breast:
38	chr11:63790736..63792785-chr11:63800297..63802100,2	K562	blood:
39	chr11:63801299..63803678-chr11:63819162..63821400,2	MCF-7	breast:
40	chr11:63824548..63827286-chr11:63828477..63832057,3	K562	blood:
41	chr11:63831163..63834275-chr11:63854365..63857011,4	K562	blood:
42	chr11:63741996..63743584-chr11:63770498..63773173,2	K562	blood:
43	chr11:63771593..63774373-chr11:63777234..63778755,2	MCF-7	breast:
44	chr11:63789285..63790804-chr11:63809733..63811420,2	K562	blood:
45	chr11:63785453..63787143-chr11:63789041..63790894,2	MCF-7	breast:
46	chr11:63844264..63846249-chr11:63850174..63851834,2	MCF-7	breast:
47	chr11:63820080..63822611-chr11:63830235..63832335,2	MCF-7	breast:
48	chr11:63808999..63812424-chr11:63814296..63816296,3	K562	blood:
49	chr11:63799424..63801976-chr11:63803879..63805403,2	K562	blood:
50	chr11:63821048..63822913-chr11:63844832..63846424,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COX8A-2	chr11:63768587-63768992	NONHSAT021929
2	lnc-FLRT1-2	chr11:63827896-63828128	ENSG00000256824.1
3	lnc-FLRT1-2	chr11:63804224-63804247	NONHSAT021933
4	lnc-COX8A-2	chr11:63769188-63769239	NONHSAT021929

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	OTUB1	hsa-miR-28-5p	chr11:63765840-63765846

Variant related genes	Relation type
ENSG00000256824	TF binding region
OTUB1	TF binding region
MACROD1	TF binding region
ENSG00000256481	TF binding region
ENSG00000256824	CpG island
OTUB1	CpG island
MACROD1	CpG island
ENSG00000256481	CpG island
ENSG00000176340	chromatin interactions
ENSG00000110583	chromatin interactions
ENSG00000256824	chromatin interactions
ENSG00000133315	chromatin interactions
ENSG00000121274	chromatin interactions
ENSG00000168439	chromatin interactions
ENSG00000167771	chromatin interactions
ENSG00000181908	chromatin interactions
ENSG00000167770	chromatin interactions
ENSG00000256481	chromatin interactions
ENSG00000256100	chromatin interactions

Extended variants
information (count: 3247 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3247 , 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	rs11231671	chr11:63761169-63761170	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10792424	chr11:63761207-63761208	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs527244612	chr11:63761269-63761270	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs540776523	chr11:63761289-63761290	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560988208	chr11:63761297-63761298	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529747031	chr11:63761300-63761301	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549986190	chr11:63761364-63761365	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569493353	chr11:63761369-63761370	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549818303	chr11:63761386-63761387	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34143455	chr11:63761406-63761407	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs36068502	chr11:63761414-63761415	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35279945	chr11:63761438-63761439	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35361996	chr11:63761443-63761444	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs36073815	chr11:63761445-63761446	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553872543	chr11:63761464-63761465	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532297859	chr11:63761547-63761548	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576741335	chr11:63761548-63761549	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs558164466	chr11:63761604-63761605	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552020752	chr11:63761648-63761649	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571319321	chr11:63761680-63761681	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188485131	chr11:63761682-63761683	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34028180	chr11:63761727-63761728	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553877503	chr11:63761773-63761774	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555900708	chr11:63761789-63761790	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575503585	chr11:63761798-63761799	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3019784	chr11:63761805-63761806	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs375215479	chr11:63761827-63761828	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536333242	chr11:63761847-63761848	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192879760	chr11:63761881-63761882	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544504432	chr11:63761951-63761952	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371383049	chr11:63761959-63761960	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139049388	chr11:63762024-63762025	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs559251815	chr11:63762027-63762028	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs571946528	chr11:63762060-63762061	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541066042	chr11:63762115-63762116	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201368063	chr11:63762195-63762196	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574729473	chr11:63762206-63762207	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560709375	chr11:63762273-63762274	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149341457	chr11:63762319-63762320	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77459372	chr11:63762330-63762331	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563160367	chr11:63762372-63762373	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540324462	chr11:63762395-63762396	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs76249827	chr11:63762489-63762490	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565684563	chr11:63762537-63762538	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs528366649	chr11:63762573-63762574	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs547803817	chr11:63762617-63762618	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376826996	chr11:63762631-63762632	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549163066	chr11:63762662-63762663	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184447143	chr11:63762669-63762670	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566075845	chr11:63762677-63762678	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21785460	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	21865298	CNVD

Chromatin state (count:3245 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63754800-63767600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:63755000-63766600	Weak transcription	Right Atrium	heart
3	chr11:63755000-63769000	Weak transcription	Fetal Kidney	kidney
4	chr11:63755200-63761200	Weak transcription	HUVEC	blood vessel
5	chr11:63755200-63762000	Weak transcription	Small Intestine	intestine
6	chr11:63755200-63766600	Weak transcription	Stomach Mucosa	stomach
7	chr11:63755200-63775200	Weak transcription	Psoas Muscle	Psoas
8	chr11:63755400-63762400	Weak transcription	Brain Substantia Nigra	brain
9	chr11:63755400-63765400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr11:63755400-63765400	Strong transcription	Fetal Stomach	stomach
11	chr11:63755400-63765600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr11:63755400-63766200	Strong transcription	Fetal Muscle Leg	muscle
13	chr11:63755400-63766200	Strong transcription	Fetal Thymus	thymus
14	chr11:63755400-63766400	Strong transcription	NHLF	lung
15	chr11:63755400-63766600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:63755600-63764800	Weak transcription	Fetal Brain Male	brain
17	chr11:63755600-63765800	Strong transcription	NHEK	skin
18	chr11:63755600-63766000	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr11:63755600-63766400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr11:63755800-63762200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:63755800-63764800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:63755800-63765000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:63755800-63766200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:63756000-63762000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr11:63756000-63762200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr11:63756000-63764400	Strong transcription	Thymus	Thymus
27	chr11:63756000-63764600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr11:63756000-63765400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
29	chr11:63756000-63765600	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:63756000-63765800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr11:63756000-63766000	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr11:63756000-63766000	Strong transcription	Fetal Brain Female	brain
33	chr11:63756000-63766000	Strong transcription	Stomach Smooth Muscle	stomach
34	chr11:63756000-63766400	Weak transcription	Fetal Heart	heart
35	chr11:63756200-63765600	Strong transcription	Fetal Muscle Trunk	muscle
36	chr11:63756200-63766200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr11:63756200-63766800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr11:63756200-63769200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:63756400-63761400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:63756400-63764200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr11:63756400-63764200	Strong transcription	Lung	lung
42	chr11:63756400-63766200	Strong transcription	Primary T helper cells fromperipheralblood	blood
43	chr11:63756400-63766400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr11:63756400-63766400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr11:63757600-63762400	Strong transcription	Placenta Amnion	Placenta Amnion
46	chr11:63757600-63762600	Strong transcription	GM12878-XiMat	blood
47	chr11:63758000-63765000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr11:63758400-63764200	Weak transcription	HSMM	muscle
49	chr11:63758400-63766200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:63758600-63766600	Strong transcription	Fetal Intestine Small	intestine

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