Variant report

Variant	esv3418266
Chromosome Location	chr11:47610276-47613374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:22)
CpG islands
(count:245)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:47612188-47612296	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr11:47611840-47611990	HUVEC	blood vessel:	n/a	n/a
3	JUN	chr11:47610939-47610953	HepG2	liver:	n/a	n/a
4	MAX	chr11:47611189-47611881	HUVEC	blood vessel:	n/a	n/a
5	MAX	chr11:47613221-47614234	NB4	blood:	n/a	chr11:47614159-47614172 chr11:47614161-47614170 chr11:47614160-47614171 chr11:47614160-47614171 chr11:47614160-47614170 chr11:47614159-47614172
6	MTA3	chr11:47613194-47613699	GM12878	blood:	n/a	n/a
7	MYBL2	chr11:47613290-47613705	HepG2	liver:	n/a	chr11:47613491-47613501
8	MYC	chr11:47611687-47611728	HUVEC	blood vessel:	n/a	n/a
9	MYC	chr11:47611462-47611680	HUVEC	blood vessel:	n/a	n/a
10	MYC	chr11:47611944-47611951	HUVEC	blood vessel:	n/a	n/a
11	MYC	chr11:47613239-47613892	NB4	blood:	n/a	n/a
12	MYC	chr11:47609113-47610308	NB4	blood:	n/a	chr11:47609697-47609707
13	NRF1	chr11:47611795-47611856	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr11:47613279-47613640	PFSK-1	brain:	n/a	n/a
15	POLR2A	chr11:47611206-47612092	HUVEC	blood vessel:	n/a	n/a
16	POLR2A	chr11:47611383-47612047	HUVEC	blood vessel:	n/a	n/a
17	POLR2A	chr11:47611892-47612100	HUVEC	blood vessel:	n/a	n/a
18	POLR2A	chr11:47610073-47610442	HepG2	liver:	n/a	n/a
19	POLR2A	chr11:47611682-47611879	HUVEC	blood vessel:	n/a	n/a
20	RAD21	chr11:47612093-47612478	H1-hESC	embryonic stem cell:	n/a	n/a
21	RUNX3	chr11:47613218-47613712	GM12878	blood:	n/a	n/a
22	RUNX3	chr11:47613199-47613668	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:47612380-47612430	PrEC	prostate:	n/a
2	chr11:47612380-47612430	PrEC	prostate:	n/a
3	chr11:47612070-47612120	Hepatocyte	liver:	n/a
4	chr11:47611780-47611830	NHDF-neo	bronchial:	n/a
5	chr11:47611236-47611286	HCM	heart:	n/a
6	chr11:47612380-47612430	AG09309	skin:	n/a
7	chr11:47612070-47612120	Hela-S3	cervix:	n/a
8	chr11:47612070-47612120	PrEC	prostate:	n/a
9	chr11:47611780-47611830	HRE	kidney:	n/a
10	chr11:47612070-47612120	ovcar-3	ovarian:	n/a
11	chr11:47611236-47611286	NH-A	brain:	n/a
12	chr11:47612070-47612120	GM12892	blood:	n/a
13	chr11:47612380-47612430	CMK	blood:	n/a
14	chr11:47611780-47611830	IMR90	lung:	fetal
15	chr11:47611780-47611830	GM19239	blood:	n/a
16	chr11:47611780-47611830	Caco-2	colon:	n/a
17	chr11:47612380-47612430	NHBE	bronchial:	n/a
18	chr11:47612070-47612120	BJ	skin:	n/a
19	chr11:47611780-47611830	AoSMC	blood vessel:	n/a
20	chr11:47612070-47612120	GM12878	blood:	n/a
21	chr11:47612380-47612430	Caco-2	colon:	n/a
22	chr11:47612380-47612430	HUVEC	blood vessel:	n/a
23	chr11:47611780-47611830	GM12891	blood:	n/a
24	chr11:47612380-47612430	Hela-S3	cervix:	n/a
25	chr11:47612070-47612120	HNPCEpiC	eye:	n/a
26	chr11:47611236-47611286	SAEC	small airway:	n/a
27	chr11:47612380-47612430	GM12878	blood:	n/a
28	chr11:47612070-47612120	ECC-1	luminal epithelium:	n/a
29	chr11:47611780-47611830	ProgFib	skin:	n/a
30	chr11:47611780-47611830	H1-hESC	embryonic stem cell:	embryo
31	chr11:47612380-47612430	HCF	heart:	n/a
32	chr11:47611780-47611830	K562	blood:	n/a
33	chr11:47612380-47612430	HL-60	blood:	n/a
34	chr11:47611780-47611830	NH-A	brain:	n/a
35	chr11:47612380-47612430	HNPCEpiC	eye:	n/a
36	chr11:47611236-47611286	GM12892	blood:	n/a
37	chr11:47612070-47612120	SK-N-MC	brain:	n/a
38	chr11:47612070-47612120	AoSMC	blood vessel:	n/a
39	chr11:47611236-47611286	ovcar-3	ovarian:	n/a
40	chr11:47612380-47612430	SKMC	muscle:	n/a
41	chr11:47611236-47611286	NT2-D1	testis:	n/a
42	chr11:47612070-47612120	HRE	kidney:	n/a
43	chr11:47612070-47612120	HepG2	liver:	n/a
44	chr11:47612070-47612120	U87	brain:	n/a
45	chr11:47612380-47612430	HRCEpiC	kidney:	n/a
46	chr11:47611780-47611830	HEEpiC	esophagus:	n/a
47	chr11:47612070-47612120	AG09319	gingival:	n/a
48	chr11:47611780-47611830	PFSK-1	brain:	n/a
49	chr11:47611780-47611830	AG04450	lung:	fetal
50	chr11:47611236-47611286	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:47612536..47615119-chr11:47621366..47624044,3	MCF-7	breast:
2	chr11:47612835..47615053-chr11:47623359..47624985,2	MCF-7	breast:
3	chr11:47612748..47614519-chr11:47788847..47791684,2	K562	blood:
4	chr11:47586895..47590126-chr11:47609798..47613644,4	MCF-7	breast:

No data

Variant related genes	Relation type
C1QTNF4	TF binding region
C1QTNF4	CpG island
ENSG00000149187	chromatin interactions
ENSG00000109920	chromatin interactions
ENSG00000110536	chromatin interactions

Extended variants
information (count: 122 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:122 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149663299	chr11:47610277-47610278	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs144968047	chr11:47610279-47610280	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs58699057	chr11:47610307-47610308	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs3029432	chr11:47610308-47610309	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553897661	chr11:47610315-47610316	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576919525	chr11:47610323-47610324	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs185671635	chr11:47610406-47610407	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs112897173	chr11:47610482-47610483	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569963671	chr11:47610483-47610484	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs190548237	chr11:47610526-47610527	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544195926	chr11:47610537-47610538	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs535798165	chr11:47610540-47610541	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373959666	chr11:47610567-47610568	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs140366535	chr11:47610569-47610570	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs529662476	chr11:47610571-47610572	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs374178389	chr11:47610588-47610589	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs150041758	chr11:47610611-47610612	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537039219	chr11:47610643-47610644	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs532223600	chr11:47610644-47610645	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs552273111	chr11:47610661-47610662	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs145300279	chr11:47610796-47610797	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs565827908	chr11:47610823-47610824	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs531889825	chr11:47611009-47611010	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs548601880	chr11:47611024-47611025	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376449097	chr11:47611071-47611072	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs533980298	chr11:47611108-47611109	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs180799689	chr11:47611141-47611142	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs570641542	chr11:47611146-47611147	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs185420118	chr11:47611148-47611149	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs11039307	chr11:47611152-47611153	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs111702042	chr11:47611159-47611160	Weak transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs555353178	chr11:47611210-47611211	Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs181310562	chr11:47611216-47611217	Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs10769279	chr11:47611316-47611317	Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs367675181	chr11:47611340-47611341	Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540258878	chr11:47611366-47611367	Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373404571	chr11:47611412-47611413	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs532108269	chr11:47611466-47611467	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs186546762	chr11:47611477-47611478	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs200189635	chr11:47611502-47611503	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs140343988	chr11:47611516-47611517	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs202156683	chr11:47611523-47611524	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs376664675	chr11:47611544-47611545	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548756083	chr11:47611553-47611554	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145222942	chr11:47611580-47611581	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs527958768	chr11:47611581-47611582	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs547659152	chr11:47611582-47611583	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200635776	chr11:47611583-47611584	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs539408097	chr11:47611585-47611586	Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs147649645	chr11:47611625-47611626	Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Obesity	20935630	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47601400-47611800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:47601400-47613400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr11:47602200-47610400	Strong transcription	Fetal Brain Female	brain
4	chr11:47603800-47612400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr11:47604000-47612000	Weak transcription	Small Intestine	intestine
6	chr11:47604400-47610800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr11:47605000-47611000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:47605600-47610800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr11:47605800-47610800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr11:47606000-47610400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr11:47606000-47611000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr11:47606000-47611400	Weak transcription	HMEC	breast
13	chr11:47606000-47614200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:47606200-47610800	Weak transcription	Fetal Heart	heart
15	chr11:47606200-47610800	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:47606200-47611200	Weak transcription	Colonic Mucosa	Colon
17	chr11:47606200-47611400	Weak transcription	NH-A	brain
18	chr11:47606200-47612000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr11:47606200-47612600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr11:47606200-47614200	Weak transcription	A549	lung
21	chr11:47606200-47614600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr11:47606400-47610600	Weak transcription	NHEK	skin
23	chr11:47606400-47610600	Weak transcription	Osteobl	bone
24	chr11:47606400-47612000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr11:47606400-47612400	Weak transcription	GM12878-XiMat	blood
26	chr11:47606600-47613400	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr11:47606800-47610800	Weak transcription	HUVEC	blood vessel
28	chr11:47606800-47611400	Weak transcription	Gastric	stomach
29	chr11:47606800-47611600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr11:47606800-47613200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:47606800-47613600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr11:47606800-47613600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr11:47607000-47610600	Weak transcription	Fetal Lung	lung
34	chr11:47607000-47610600	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr11:47607000-47610800	Weak transcription	Rectal Smooth Muscle	rectum
36	chr11:47607000-47611000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:47607000-47611000	Weak transcription	Left Ventricle	heart
38	chr11:47607000-47611200	Weak transcription	Psoas Muscle	Psoas
39	chr11:47607000-47611600	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr11:47607000-47611600	Weak transcription	Pancreas	Pancrea
41	chr11:47607000-47612200	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr11:47607000-47612800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr11:47607000-47613200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:47607000-47613200	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr11:47607000-47613400	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr11:47607000-47613400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr11:47607000-47632800	Weak transcription	Dnd41	blood
48	chr11:47607200-47612600	Weak transcription	Fetal Thymus	thymus
49	chr11:47607200-47613600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr11:47607600-47613000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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