Variant report

Variant	esv3377128
Chromosome Location	chr11:65836776-65839324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:427)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:65837178-65837719	GM12878	blood:	n/a	n/a
2	ATF2	chr11:65836331-65836856	GM12878	blood:	n/a	n/a
3	ATF2	chr11:65836307-65836870	GM12878	blood:	n/a	n/a
4	BACH1	chr11:65837420-65837880	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr11:65836882-65837136	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr11:65836667-65837492	A549	lung:	n/a	chr11:65837302-65837315
7	BCL3	chr11:65837164-65837986	GM12878	blood:	n/a	chr11:65837302-65837315
8	BCL3	chr11:65836494-65837558	A549	lung:	n/a	chr11:65837302-65837315
9	BCLAF1	chr11:65836969-65837873	GM12878	blood:	n/a	chr11:65837302-65837315
10	BHLHE40	chr11:65836449-65837033	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:65837450-65837880	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:65837661-65837884	K562	blood:	n/a	n/a
13	CCNT2	chr11:65837208-65838564	K562	blood:	n/a	n/a
14	CEBPB	chr11:65838610-65838896	A549	lung:	n/a	chr11:65838693-65838704
15	CEBPB	chr11:65837233-65837326	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr11:65838572-65838872	K562	blood:	n/a	chr11:65838693-65838704
17	CEBPB	chr11:65838574-65838803	HepG2	liver:	n/a	chr11:65838693-65838704
18	CEBPB	chr11:65838503-65838945	Hela-S3	cervix:	n/a	chr11:65838693-65838704
19	CEBPB	chr11:65838491-65838876	K562	blood:	n/a	chr11:65838693-65838704
20	CEBPD	chr11:65837257-65837603	HepG2	liver:	n/a	n/a
21	CEBPD	chr11:65837639-65837944	HepG2	liver:	n/a	n/a
22	CHD1	chr11:65839168-65839217	GM12878	blood:	n/a	n/a
23	CHD1	chr11:65837824-65838085	GM12878	blood:	n/a	n/a
24	CHD1	chr11:65836785-65836985	GM12878	blood:	n/a	n/a
25	CHD1	chr11:65838849-65838949	GM12878	blood:	n/a	n/a
26	CHD1	chr11:65838563-65838629	GM12878	blood:	n/a	n/a
27	CHD2	chr11:65836506-65837093	GM12878	blood:	n/a	n/a
28	CHD2	chr11:65838208-65838226	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr11:65837356-65837913	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr11:65837637-65837928	K562	blood:	n/a	n/a
31	CHD2	chr11:65838801-65839051	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr11:65837508-65837978	GM12878	blood:	n/a	n/a
33	CHD2	chr11:65837646-65837768	HepG2	liver:	n/a	n/a
34	CREB1	chr11:65836920-65838464	HepG2	liver:	n/a	n/a
35	CREB1	chr11:65837194-65838013	A549	lung:	n/a	n/a
36	CREB1	chr11:65836896-65838012	GM12878	blood:	n/a	n/a
37	CREB1	chr11:65838043-65838411	A549	lung:	n/a	n/a
38	CTCF	chr11:65837000-65837150	SAEC	small airway:	n/a	n/a
39	CTCF	chr11:65836910-65837108	GM13977	blood:	n/a	n/a
40	CTCF	chr11:65836880-65837030	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr11:65836955-65837036	GM10248	blood:	n/a	n/a
42	CTCF	chr11:65836960-65837110	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr11:65837040-65837190	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr11:65837300-65837450	GM12873	blood:	n/a	n/a
45	CTCF	chr11:65837027-65837045	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr11:65838155-65838197	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:65836965-65837034	LNCaP	prostate:	n/a	n/a
48	CTCF	chr11:65836960-65837110	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr11:65837300-65837450	RPTEC	kidney:	n/a	n/a
50	CTCF	chr11:65836894-65837027	Spleen_OC	spleen:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:65836743-65836793	HPAEpiC	pulmonary alveolar:	n/a
2	chr11:65838645-65838695	NH-A	brain:	n/a
3	chr11:65837996-65838046	NB4	blood:	n/a
4	chr11:65837255-65837305	SKMC	muscle:	n/a
5	chr11:65838645-65838695	GM12878	blood:	n/a
6	chr11:65836743-65836793	ECC-1	luminal epithelium:	n/a
7	chr11:65837595-65837645	AG04450	lung:	fetal
8	chr11:65837996-65838046	K562	blood:	n/a
9	chr11:65836743-65836793	NT2-D1	testis:	n/a
10	chr11:65836743-65836793	Jurkat	blood:	n/a
11	chr11:65836743-65836793	HCT-116	colon:	n/a
12	chr11:65837996-65838046	AG09309	skin:	n/a
13	chr11:65837194-65837244	HEK293	kidney:	embryo
14	chr11:65836743-65836793	GM06990	blood:	n/a
15	chr11:65838645-65838695	GM12891	blood:	n/a
16	chr11:65838645-65838695	GM19239	blood:	n/a
17	chr11:65837996-65838046	SKMC	muscle:	n/a
18	chr11:65836743-65836793	AG09319	gingival:	n/a
19	chr11:65837194-65837244	HRE	kidney:	n/a
20	chr11:65836743-65836793	AG04450	lung:	fetal
21	chr11:65837255-65837305	NT2-D1	testis:	n/a
22	chr11:65838237-65838287	SK-N-SH	brain:	n/a
23	chr11:65837194-65837244	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:65838645-65838695	HCM	heart:	n/a
25	chr11:65837255-65837305	ovcar-3	ovarian:	n/a
26	chr11:65837194-65837244	HIPEpiC	eye:	n/a
27	chr11:65837595-65837645	Jurkat	blood:	n/a
28	chr11:65837255-65837305	HRE	kidney:	n/a
29	chr11:65837194-65837244	MCF10A-Er-Src	breast:	n/a
30	chr11:65837595-65837645	HPAEpiC	pulmonary alveolar:	n/a
31	chr11:65837595-65837645	Hepatocyte	liver:	n/a
32	chr11:65837194-65837244	NHBE	bronchial:	n/a
33	chr11:65837996-65838046	U87	brain:	n/a
34	chr11:65838237-65838287	HCT-116	colon:	n/a
35	chr11:65837255-65837305	LNCaP	prostate:	n/a
36	chr11:65837194-65837244	HCT-116	colon:	n/a
37	chr11:65837595-65837645	LNCaP	prostate:	n/a
38	chr11:65837595-65837645	GM12892	blood:	n/a
39	chr11:65837194-65837244	ProgFib	skin:	n/a
40	chr11:65837996-65838046	HCM	heart:	n/a
41	chr11:65837255-65837305	MCF10A-Er-Src	breast:	n/a
42	chr11:65837996-65838046	SK-N-SH	brain:	n/a
43	chr11:65837194-65837244	HepG2	liver:	n/a
44	chr11:65838237-65838287	PANC-1	pancreas:	n/a
45	chr11:65837595-65837645	MCF-7	breast:	n/a
46	chr11:65837996-65838046	ProgFib	skin:	n/a
47	chr11:65836743-65836793	H1-hESC	embryonic stem cell:	embryo
48	chr11:65838645-65838695	HCPEpiC	choroid plexus:	n/a
49	chr11:65838645-65838695	BE2_C	brain:	n/a
50	chr11:65837194-65837244	HCM	heart:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:65839190..65841660-chr11:65977914..65980146,2	K562	blood:
2	chr11:65654814..65656550-chr11:65837621..65839885,2	MCF-7	breast:
3	chr11:65638895..65641565-chr11:65834356..65837225,2	K562	blood:
4	chr11:65812922..65815510-chr11:65837744..65839701,2	K562	blood:
5	chr11:65835858..65838956-chr11:66027814..66030508,4	MCF-7	breast:
6	chr11:65788482..65791914-chr11:65833749..65837289,3	MCF-7	breast:
7	chr11:65779081..65782393-chr11:65836476..65839425,3	MCF-7	breast:
8	chr11:65768121..65772581-chr11:65835630..65838620,4	MCF-7	breast:
9	chr11:65656719..65659047-chr11:65835301..65837715,2	MCF-7	breast:
10	chr11:65826244..65833224-chr11:65834439..65839387,11	MCF-7	breast:
11	chr11:65788387..65789947-chr11:65837601..65839297,2	K562	blood:
12	chr11:65836209..65839625-chr11:66023244..66027607,5	K562	blood:
13	chr11:65654924..65661575-chr11:65833688..65838665,10	K562	blood:
14	chr11:65623430..65625691-chr11:65837839..65839866,2	K562	blood:
15	chr11:65625072..65626937-chr11:65835477..65837832,2	K562	blood:
16	chr11:65685063..65688035-chr11:65836071..65837888,2	MCF-7	breast:
17	chr11:65837641..65839546-chr11:66050688..66053288,2	K562	blood:
18	chr11:65816864..65823380-chr11:65832037..65840391,16	MCF-7	breast:
19	chr11:65836782..65838328-chr20:49347114..49348947,2	MCF-7	breast:
20	chr11:65836630..65840121-chr11:66032259..66035828,5	MCF-7	breast:
21	chr11:65836209..65839676-chr11:66023244..66028603,5	K562	blood:
22	chr11:65665582..65668888-chr11:65835107..65838015,3	K562	blood:
23	chr11:65837683..65838307-chr6:26196783..26197662,2	Hela-S3	cervix:
24	chr11:65654924..65660442-chr11:65834310..65838665,6	K562	blood:
25	chr11:65837353..65839732-chr11:66024702..66027312,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000255038	TF binding region
PACS1	TF binding region
ENSG00000255038	CpG island
PACS1	CpG island
ENSG00000175602	chromatin interactions
ENSG00000087365	chromatin interactions
ENSG00000238752	chromatin interactions
ENSG00000175294	chromatin interactions
ENSG00000172500	chromatin interactions
ENSG00000175592	chromatin interactions
ENSG00000254855	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000175573	chromatin interactions
ENSG00000172638	chromatin interactions
ENSG00000175334	chromatin interactions
ENSG00000175550	chromatin interactions
ENSG00000175376	chromatin interactions
ENSG00000254461	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000174996	chromatin interactions
ENSG00000175229	chromatin interactions
ENSG00000254762	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000175315	chromatin interactions

Extended variants
information (count: 62 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:62 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528872693	chr11:65836847-65836848	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
2	rs147419539	chr11:65836864-65836865	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
3	rs576849082	chr11:65836884-65836885	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
4	rs139226719	chr11:65836899-65836900	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
5	rs187690282	chr11:65836925-65836926	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
6	rs532140628	chr11:65836966-65836967	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
7	rs551852624	chr11:65837022-65837023	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
8	rs2277303	chr11:65837056-65837057	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
9	rs375956387	chr11:65837087-65837088	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
10	rs565799567	chr11:65837131-65837132	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
11	rs534683130	chr11:65837137-65837138	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
12	rs151185965	chr11:65837138-65837139	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
13	rs548554123	chr11:65837153-65837154	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
14	rs554448996	chr11:65837197-65837198	Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
15	rs567859900	chr11:65837311-65837312	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
16	rs369034703	chr11:65837381-65837382	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
17	rs556827902	chr11:65837455-65837456	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
18	rs2254388	chr11:65837599-65837600	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	18 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs545408979	chr11:65837623-65837624	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
20	rs2376231	chr11:65837679-65837680	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
21	rs572241175	chr11:65837842-65837843	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
22	rs149876307	chr11:65837928-65837929	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
23	rs75352646	chr11:65838059-65838060	Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
24	rs369233658	chr11:65838061-65838062	Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
25	rs543611409	chr11:65838124-65838125	Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
26	rs543210951	chr11:65838142-65838143	Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
27	rs563612549	chr11:65838203-65838204	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
28	rs532276860	chr11:65838326-65838327	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	18 gene(s)	Overlapped CNVs	n/a
29	rs552228058	chr11:65838343-65838344	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
30	rs373934734	chr11:65838406-65838407	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
31	rs565673155	chr11:65838458-65838459	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
32	rs528244945	chr11:65838511-65838512	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
33	rs11823618	chr11:65838530-65838531	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
34	rs144912153	chr11:65838532-65838533	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
35	rs77867801	chr11:65838572-65838573	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
36	rs550079141	chr11:65838623-65838624	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs370587938	chr11:65838646-65838647	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs570356803	chr11:65838661-65838662	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs148632581	chr11:65838678-65838679	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs531940251	chr11:65838688-65838689	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
41	rs558568231	chr11:65838712-65838713	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs572104175	chr11:65838735-65838736	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
43	rs570964148	chr11:65838787-65838788	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
44	rs534653144	chr11:65838832-65838833	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
45	rs35526559	chr11:65838845-65838846	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
46	rs187871943	chr11:65838944-65838945	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
47	rs574802073	chr11:65838947-65838948	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
48	rs543622554	chr11:65838953-65838954	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
49	rs563314340	chr11:65838964-65838965	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
50	rs577101209	chr11:65838977-65838978	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:555 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65828200-65838000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:65829400-65836800	Strong transcription	Dnd41	blood
3	chr11:65831800-65836800	Weak transcription	Small Intestine	intestine
4	chr11:65832400-65836800	Strong transcription	Sigmoid Colon	Sigmoid Colon
5	chr11:65832800-65837000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:65833000-65836800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:65833800-65836800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr11:65833800-65836800	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:65833800-65836800	Genic enhancers	Liver	Liver
10	chr11:65834000-65836800	Genic enhancers	Primary B cells from peripheral blood	blood
11	chr11:65834000-65836800	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr11:65834000-65836800	Genic enhancers	Primary T helper cells PMA-I stimulated	--
13	chr11:65835000-65837000	Genic enhancers	Primary T cells fromperipheralblood	blood
14	chr11:65835200-65836800	Genic enhancers	Primary T helper cells fromperipheralblood	blood
15	chr11:65835200-65836800	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr11:65835200-65836800	Genic enhancers	Fetal Muscle Trunk	muscle
17	chr11:65835200-65837000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr11:65835400-65836800	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr11:65835400-65836800	Genic enhancers	Brain Substantia Nigra	brain
20	chr11:65835400-65837000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr11:65835400-65837000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
22	chr11:65835400-65837000	Genic enhancers	Fetal Muscle Leg	muscle
23	chr11:65835400-65837000	Genic enhancers	Placenta	Placenta
24	chr11:65835400-65837000	Genic enhancers	Fetal Thymus	thymus
25	chr11:65835400-65837200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr11:65835400-65837200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr11:65835600-65836800	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr11:65835600-65836800	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr11:65835600-65836800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr11:65835600-65836800	Genic enhancers	Brain Cingulate Gyrus	brain
31	chr11:65835600-65836800	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr11:65835600-65836800	Genic enhancers	Esophagus	oesophagus
33	chr11:65835600-65837000	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr11:65835600-65837000	Genic enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr11:65835600-65837000	Genic enhancers	Gastric	stomach
36	chr11:65835600-65837000	Genic enhancers	Left Ventricle	heart
37	chr11:65835600-65837000	Genic enhancers	Right Atrium	heart
38	chr11:65835800-65836800	Enhancers	Primary B cells from cord blood	blood
39	chr11:65835800-65836800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr11:65835800-65836800	Genic enhancers	Placenta Amnion	Placenta Amnion
41	chr11:65835800-65836800	Genic enhancers	K562	blood
42	chr11:65835800-65836800	Genic enhancers	Osteobl	bone
43	chr11:65835800-65837000	Transcr. at gene 5' and 3'	Fetal Brain Female	brain
44	chr11:65835800-65837000	Genic enhancers	Fetal Lung	lung
45	chr11:65835800-65837200	Weak transcription	Aorta	Aorta
46	chr11:65835800-65837200	Weak transcription	Ovary	ovary
47	chr11:65836000-65836800	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr11:65836000-65836800	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr11:65836000-65836800	Genic enhancers	HUES48 Cell Line	embryonic stem cell
50	chr11:65836000-65836800	Genic enhancers	iPS-18 Cell Line	embryonic stem cell

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