Variant report

Variant	esv3374722
Chromosome Location	chr11:75060004-75064302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:783)
CpG islands
(count:366)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:783 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:75063572-75063891	K562	blood:	n/a	n/a
2	ARID3A	chr11:75063293-75063623	HepG2	liver:	n/a	n/a
3	ATF3	chr11:75062479-75062768	K562	blood:	n/a	chr11:75062678-75062692
4	BACH1	chr11:75061793-75062599	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:75062819-75063623	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr11:75062756-75063244	A549	lung:	n/a	chr11:75062935-75062948
7	BHLHE40	chr11:75060747-75060924	K562	blood:	n/a	n/a
8	BHLHE40	chr11:75061839-75062470	GM12878	blood:	n/a	chr11:75061927-75061943 chr11:75062400-75062416
9	BHLHE40	chr11:75061779-75063645	K562	blood:	n/a	chr11:75061927-75061943 chr11:75062400-75062416 chr11:75063455-75063471
10	BHLHE40	chr11:75062797-75063297	GM12878	blood:	n/a	n/a
11	BRCA1	chr11:75063471-75063502	HepG2	liver:	n/a	n/a
12	CBX3	chr11:75062799-75063732	K562	blood:	n/a	n/a
13	CBX3	chr11:75061720-75062792	K562	blood:	n/a	n/a
14	CCNT2	chr11:75062211-75063620	K562	blood:	n/a	chr11:75062986-75062995 chr11:75063348-75063357
15	CEBPB	chr11:75063190-75063300	K562	blood:	n/a	n/a
16	CEBPB	chr11:75060262-75060587	HepG2	liver:	n/a	chr11:75060413-75060424
17	CEBPB	chr11:75060348-75060644	K562	blood:	n/a	chr11:75060413-75060424
18	CEBPD	chr11:75063177-75063653	K562	blood:	n/a	n/a
19	CEBPD	chr11:75062828-75063622	HepG2	liver:	n/a	n/a
20	CHD1	chr11:75063530-75063669	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr11:75062932-75063120	GM12878	blood:	n/a	n/a
22	CHD2	chr11:75063411-75063513	HepG2	liver:	n/a	n/a
23	CHD2	chr11:75062534-75062661	HepG2	liver:	n/a	n/a
24	CHD2	chr11:75062628-75063033	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr11:75062809-75063518	GM12878	blood:	n/a	n/a
26	CHD2	chr11:75063287-75063622	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr11:75061908-75062025	HepG2	liver:	n/a	n/a
28	CHD2	chr11:75062923-75063130	HepG2	liver:	n/a	n/a
29	CHD2	chr11:75062304-75063578	K562	blood:	n/a	n/a
30	CHD2	chr11:75061941-75062562	GM12878	blood:	n/a	n/a
31	CREB1	chr11:75062027-75063172	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr11:75062095-75063413	A549	lung:	n/a	n/a
33	CREB1	chr11:75061754-75063276	K562	blood:	n/a	n/a
34	CTBP2	chr11:75061720-75063688	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr11:75061775-75061940	Medullo	brain:	n/a	n/a
36	CTCF	chr11:75061720-75061870	MCF-7	breast:	n/a	n/a
37	CTCF	chr11:75062664-75062721	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr11:75061980-75062036	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr11:75061860-75062010	GM12872	blood:	n/a	n/a
40	CTCF	chr11:75061800-75061971	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr11:75062200-75062350	SAEC	small airway:	n/a	n/a
42	CTCF	chr11:75061800-75061950	GM12875	blood:	n/a	n/a
43	CTCF	chr11:75063400-75063550	A549	lung:	n/a	chr11:75063462-75063471 chr11:75063459-75063477
44	CTCF	chr11:75061800-75061950	Caco-2	colon:	n/a	n/a
45	CTCF	chr11:75063408-75063537	Pancreas_OC	pancreas:	n/a	chr11:75063462-75063471 chr11:75063459-75063477
46	CTCF	chr11:75061800-75061950	GM12865	blood:	n/a	n/a
47	CTCF	chr11:75063360-75063510	BJ	skin:	n/a	chr11:75063462-75063471 chr11:75063459-75063477
48	CTCF	chr11:75062600-75062750	SK-N-SH_RA	brain:	n/a	chr11:75062708-75062726 chr11:75062711-75062724
49	CTCF	chr11:75062600-75062750	Hela-S3	cervix:	n/a	chr11:75062708-75062726 chr11:75062711-75062724
50	CTCF	chr11:75062520-75062670	GM12873	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:75062225-75062275	HEEpiC	esophagus:	n/a
2	chr11:75063246-75063296	HUVEC	blood vessel:	n/a
3	chr11:75063246-75063296	NT2-D1	testis:	n/a
4	chr11:75063246-75063296	AoSMC	blood vessel:	n/a
5	chr11:75061838-75061888	NHBE	bronchial:	n/a
6	chr11:75063913-75063963	SKMC	muscle:	n/a
7	chr11:75063246-75063296	ProgFib	skin:	n/a
8	chr11:75063913-75063963	AG09319	gingival:	n/a
9	chr11:75063569-75063619	AG04450	lung:	fetal
10	chr11:75063246-75063296	MCF10A-Er-Src	breast:	n/a
11	chr11:75062600-75062650	K562	blood:	n/a
12	chr11:75062225-75062275	H1-hESC	embryonic stem cell:	embryo
13	chr11:75063569-75063619	PFSK-1	brain:	n/a
14	chr11:75062600-75062650	HCF	heart:	n/a
15	chr11:75063569-75063619	NB4	blood:	n/a
16	chr11:75063913-75063963	HRPEpiC	eye:	n/a
17	chr11:75063913-75063963	IMR90	lung:	fetal
18	chr11:75063913-75063963	HIPEpiC	eye:	n/a
19	chr11:75062600-75062650	H1-hESC	embryonic stem cell:	embryo
20	chr11:75062225-75062275	K562	blood:	n/a
21	chr11:75062600-75062650	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:75063913-75063963	HRCEpiC	kidney:	n/a
23	chr11:75063246-75063296	GM12891	blood:	n/a
24	chr11:75062225-75062275	PrEC	prostate:	n/a
25	chr11:75063569-75063619	MCF10A-Er-Src	breast:	n/a
26	chr11:75062225-75062275	NT2-D1	testis:	n/a
27	chr11:75063569-75063619	NHBE	bronchial:	n/a
28	chr11:75063569-75063619	MCF-7	breast:	n/a
29	chr11:75062225-75062275	Hepatocyte	liver:	n/a
30	chr11:75062225-75062275	AG04449	skin:	fetal
31	chr11:75063246-75063296	HAEpiC	amniotic membrane:	n/a
32	chr11:75062225-75062275	HNPCEpiC	eye:	n/a
33	chr11:75063569-75063619	AoSMC	blood vessel:	n/a
34	chr11:75063246-75063296	AG04449	skin:	fetal
35	chr11:75063246-75063296	T-47D	breast:	n/a
36	chr11:75061838-75061888	AG10803	skin:	n/a
37	chr11:75062600-75062650	U87	brain:	n/a
38	chr11:75063569-75063619	H1-hESC	embryonic stem cell:	embryo
39	chr11:75062225-75062275	ECC-1	luminal epithelium:	n/a
40	chr11:75062600-75062650	PANC-1	pancreas:	n/a
41	chr11:75061838-75061888	Hepatocyte	liver:	n/a
42	chr11:75063913-75063963	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:75063913-75063963	GM06990	blood:	n/a
44	chr11:75061838-75061888	HepG2	liver:	n/a
45	chr11:75062225-75062275	GM06990	blood:	n/a
46	chr11:75063246-75063296	SAEC	small airway:	n/a
47	chr11:75063913-75063963	U87	brain:	n/a
48	chr11:75063569-75063619	Jurkat	blood:	n/a
49	chr11:75061838-75061888	HNPCEpiC	eye:	n/a
50	chr11:75063569-75063619	HL-60	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:75063194..75065749-chr11:75140167..75143127,2	MCF-7	breast:
2	chr11:75039534..75040119-chr11:75061306..75062290,2	MCF-7	breast:
3	chr11:75061972..75065288-chr11:75110522..75113942,5	K562	blood:
4	chr11:75043210..75047420-chr11:75061230..75064804,5	MCF-7	breast:
5	chr11:75063188..75064014-chr11:124823671..124824309,2	HCT-116	colon:
6	chr11:75061780..75064300-chr11:75109349..75111939,3	MCF-7	breast:
7	chr11:75044487..75045050-chr11:75060430..75061020,2	MCF-7	breast:
8	chr11:75041535..75043406-chr11:75058885..75060928,2	K562	blood:
9	chr11:75064179..75065852-chr11:75082036..75083611,2	MCF-7	breast:
10	chr11:75056062..75061130-chr11:75109293..75114170,7	MCF-7	breast:

No data

Variant related genes	Relation type
ARRB1	TF binding region
ARRB1	CpG island
ENSG00000199090	chromatin interactions
ENSG00000149273	chromatin interactions
ENSG00000206941	chromatin interactions
ENSG00000149243	chromatin interactions
ENSG00000149548	chromatin interactions

Extended variants
information (count: 141 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:141 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148455764	chr11:75060060-75060061	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs551079362	chr11:75060111-75060112	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs181849811	chr11:75060132-75060133	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567010979	chr11:75060147-75060148	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs538857060	chr11:75060193-75060194	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs35948518	chr11:75060198-75060199	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs542985802	chr11:75060221-75060222	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186411388	chr11:75060234-75060235	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544621961	chr11:75060277-75060278	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs554975106	chr11:75060278-75060279	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544654607	chr11:75060281-75060282	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs574995532	chr11:75060303-75060304	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs34416927	chr11:75060387-75060388	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs560563556	chr11:75060396-75060397	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs141764634	chr11:75060413-75060414	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs181443286	chr11:75060462-75060463	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373422729	chr11:75060480-75060481	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs150585821	chr11:75060492-75060493	Genic enhancers Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530685309	chr11:75060609-75060610	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs550174229	chr11:75060629-75060630	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs566884095	chr11:75060630-75060631	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs2508626	chr11:75060683-75060684	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs35273882	chr11:75060700-75060701	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs58959842	chr11:75060757-75060758	Transcr. at gene 5' and 3' Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs546337335	chr11:75060825-75060826	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs566437678	chr11:75060842-75060843	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs539256706	chr11:75060884-75060885	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs187028198	chr11:75060913-75060914	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs569555955	chr11:75060940-75060941	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs538505232	chr11:75060978-75060979	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555005614	chr11:75061033-75061034	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs144192249	chr11:75061044-75061045	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs35404251	chr11:75061071-75061072	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115615153	chr11:75061122-75061123	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs577243267	chr11:75061125-75061126	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs34749024	chr11:75061150-75061151	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs191017572	chr11:75061337-75061338	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376777528	chr11:75061338-75061339	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs377391770	chr11:75061360-75061361	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183285376	chr11:75061390-75061391	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs544057535	chr11:75061414-75061415	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs370843895	chr11:75061438-75061439	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560849361	chr11:75061451-75061452	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529683630	chr11:75061470-75061471	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs140059292	chr11:75061508-75061509	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs565236110	chr11:75061528-75061529	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560222650	chr11:75061533-75061534	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532081726	chr11:75061572-75061573	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368671902	chr11:75061585-75061586	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374505574	chr11:75061699-75061700	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD

Chromatin state (count:727 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75039400-75060800	Enhancers	Placenta	Placenta
2	chr11:75044200-75060400	Genic enhancers	Fetal Stomach	stomach
3	chr11:75046400-75061200	Enhancers	Fetal Thymus	thymus
4	chr11:75046800-75060200	Enhancers	Brain Anterior Caudate	brain
5	chr11:75046800-75061600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr11:75047000-75061200	Enhancers	Left Ventricle	heart
7	chr11:75047000-75061200	Enhancers	Stomach Mucosa	stomach
8	chr11:75047200-75060400	Enhancers	Brain Angular Gyrus	brain
9	chr11:75047600-75060600	Enhancers	Right Atrium	heart
10	chr11:75047800-75060600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:75047800-75060800	Genic enhancers	Fetal Intestine Small	intestine
12	chr11:75048000-75061600	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr11:75048400-75061000	Enhancers	Liver	Liver
14	chr11:75051600-75060400	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr11:75051800-75060600	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr11:75052200-75060200	Enhancers	Brain Cingulate Gyrus	brain
17	chr11:75052200-75061200	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr11:75052200-75061400	Enhancers	Primary T cells fromperipheralblood	blood
19	chr11:75052400-75061200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr11:75052400-75061200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr11:75052400-75061800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr11:75053000-75060200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr11:75053400-75061600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:75054600-75062000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr11:75055000-75060400	Enhancers	Dnd41	blood
26	chr11:75055400-75060400	Genic enhancers	Fetal Intestine Large	intestine
27	chr11:75055400-75061400	Enhancers	Right Ventricle	heart
28	chr11:75055600-75061800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:75055800-75060200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr11:75056000-75060200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr11:75056000-75060200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
32	chr11:75056000-75060200	Enhancers	Brain Hippocampus Middle	brain
33	chr11:75056000-75060400	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr11:75056000-75061600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr11:75056200-75060200	Enhancers	Brain Substantia Nigra	brain
36	chr11:75056200-75062000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
37	chr11:75056400-75060400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr11:75056600-75060800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:75056600-75061800	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr11:75056800-75060800	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
41	chr11:75057000-75060600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:75057200-75060200	Enhancers	Fetal Brain Female	brain
43	chr11:75057200-75060400	Enhancers	HUVEC	blood vessel
44	chr11:75057200-75060800	Enhancers	Fetal Muscle Leg	muscle
45	chr11:75057200-75062000	Enhancers	Fetal Heart	heart
46	chr11:75057400-75060600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr11:75057400-75061200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr11:75057400-75061800	Weak transcription	Primary B cells from peripheral blood	blood
49	chr11:75057400-75061800	Enhancers	NHDF-Ad	bronchial
50	chr11:75057600-75060400	Enhancers	Primary hematopoietic stem cells	blood

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