Variant report

Variant	nsv897701
Chromosome Location	chr11:64501991-64520569
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1038)
CpG islands
(count:1956)
Chromatin interactive
region (count:35)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:64513600-64513686	K562	blood:	n/a	n/a
2	ATF3	chr11:64510328-64510535	HepG2	liver:	n/a	chr11:64510479-64510499 chr11:64510483-64510492 chr11:64510478-64510487
3	BACH1	chr11:64511396-64511458	K562	blood:	n/a	n/a
4	BACH1	chr11:64507890-64507909	K562	blood:	n/a	n/a
5	BACH1	chr11:64513459-64513729	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:64508915-64509052	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:64510381-64510621	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:64511055-64512010	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr11:64511109-64511713	A549	lung:	n/a	n/a
10	BHLHE40	chr11:64512846-64512859	K562	blood:	n/a	n/a
11	BHLHE40	chr11:64510346-64510615	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:64510067-64510703	K562	blood:	n/a	n/a
13	BHLHE40	chr11:64513448-64513525	K562	blood:	n/a	n/a
14	BHLHE40	chr11:64511125-64511741	GM12878	blood:	n/a	chr11:64511142-64511158
15	BHLHE40	chr11:64511121-64511761	K562	blood:	n/a	chr11:64511142-64511158
16	BHLHE40	chr11:64513168-64513196	K562	blood:	n/a	n/a
17	BHLHE40	chr11:64512457-64512883	GM12878	blood:	n/a	n/a
18	BRCA1	chr11:64510379-64510554	HepG2	liver:	n/a	n/a
19	BRCA1	chr11:64510425-64510605	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr11:64510468-64510655	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr11:64519031-64519387	K562	blood:	n/a	n/a
22	CBX3	chr11:64510875-64512128	K562	blood:	n/a	n/a
23	CBX3	chr11:64510269-64510668	K562	blood:	n/a	n/a
24	CBX3	chr11:64509876-64510216	K562	blood:	n/a	n/a
25	CBX3	chr11:64512706-64513441	K562	blood:	n/a	n/a
26	CBX3	chr11:64519075-64519394	K562	blood:	n/a	n/a
27	CCNT2	chr11:64509892-64511770	K562	blood:	n/a	chr11:64511158-64511167
28	CCNT2	chr11:64513475-64513757	K562	blood:	n/a	chr11:64513718-64513727 chr11:64513614-64513623
29	CCNT2	chr11:64512116-64513111	K562	blood:	n/a	chr11:64512601-64512610 chr11:64512965-64512974 chr11:64512474-64512483
30	CEBPB	chr11:64510379-64510764	K562	blood:	n/a	chr11:64510562-64510573
31	CEBPB	chr11:64510342-64510863	K562	blood:	n/a	chr11:64510562-64510573
32	CEBPB	chr11:64510254-64510931	A549	lung:	n/a	chr11:64510562-64510573
33	CEBPB	chr11:64519150-64519480	HepG2	liver:	n/a	chr11:64519322-64519333
34	CEBPB	chr11:64510330-64510798	ECC-1	luminal epithelium:	n/a	chr11:64510562-64510573
35	CEBPB	chr11:64510354-64510810	Hela-S3	cervix:	n/a	chr11:64510562-64510573
36	CEBPB	chr11:64510419-64510743	HepG2	liver:	n/a	chr11:64510562-64510573
37	CEBPB	chr11:64510381-64510756	A549	lung:	n/a	chr11:64510562-64510573
38	CEBPB	chr11:64507004-64507007	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr11:64519228-64519409	K562	blood:	n/a	chr11:64519322-64519333
40	CEBPB	chr11:64510375-64510756	HepG2	liver:	n/a	chr11:64510562-64510573
41	CEBPB	chr11:64510395-64510754	IMR90	lung:	n/a	chr11:64510562-64510573
42	CEBPB	chr11:64510403-64510797	ECC-1	luminal epithelium:	n/a	chr11:64510562-64510573
43	CEBPB	chr11:64510348-64510877	H1-hESC	embryonic stem cell:	n/a	chr11:64510562-64510573
44	CEBPB	chr11:64510385-64510748	HepG2	liver:	n/a	chr11:64510562-64510573
45	CEBPB	chr11:64510343-64510748	MCF-7	breast:	n/a	chr11:64510562-64510573
46	CEBPB	chr11:64510455-64510760	A549	lung:	n/a	chr11:64510562-64510573
47	CEBPB	chr11:64519271-64519343	IMR90	lung:	n/a	chr11:64519322-64519333
48	CEBPB	chr11:64519145-64519490	HepG2	liver:	n/a	chr11:64519322-64519333
49	CEBPB	chr11:64511226-64511308	K562	blood:	n/a	n/a
50	CEBPB	chr11:64510422-64510688	HepG2	liver:	n/a	chr11:64510562-64510573

(count:1956 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64511324-64511374	HRPEpiC	eye:	n/a
2	chr11:64509084-64509134	SK-N-SH	brain:	n/a
3	chr11:64511624-64511674	HCT-116	colon:	n/a
4	chr11:64510112-64510162	AG04450	lung:	fetal
5	chr11:64511324-64511374	HRPEpiC	eye:	n/a
6	chr11:64509084-64509134	SK-N-SH	brain:	n/a
7	chr11:64511624-64511674	HCT-116	colon:	n/a
8	chr11:64510112-64510162	AG04450	lung:	fetal
9	chr11:64510843-64510893	NB4	blood:	n/a
10	chr11:64513809-64513859	LNCaP	prostate:	n/a
11	chr11:64513056-64513106	HepG2	liver:	n/a
12	chr11:64513289-64513339	PANC-1	pancreas:	n/a
13	chr11:64513809-64513859	PANC-1	pancreas:	n/a
14	chr11:64509592-64509642	GM12878	blood:	n/a
15	chr11:64508056-64508106	GM12892	blood:	n/a
16	chr11:64508509-64508559	SAEC	small airway:	n/a
17	chr11:64509592-64509642	Hela-S3	cervix:	n/a
18	chr11:64511786-64511836	IMR90	lung:	fetal
19	chr11:64509084-64509134	Caco-2	colon:	n/a
20	chr11:64507260-64507310	SK-N-MC	brain:	n/a
21	chr11:64512032-64512082	Jurkat	blood:	n/a
22	chr11:64513068-64513118	MCF10A-Er-Src	breast:	n/a
23	chr11:64510112-64510162	SK-N-MC	brain:	n/a
24	chr11:64514658-64514708	MCF10A-Er-Src	breast:	n/a
25	chr11:64511624-64511674	ovcar-3	ovarian:	n/a
26	chr11:64507835-64507885	HMEC	breast:	n/a
27	chr11:64511971-64512021	HEEpiC	esophagus:	n/a
28	chr11:64510843-64510893	HPAEpiC	pulmonary alveolar:	n/a
29	chr11:64512197-64512247	NHDF-neo	bronchial:	n/a
30	chr11:64513068-64513118	HepG2	liver:	n/a
31	chr11:64513289-64513339	HAEpiC	amniotic membrane:	n/a
32	chr11:64512197-64512247	GM19239	blood:	n/a
33	chr11:64508421-64508471	U87	brain:	n/a
34	chr11:64508108-64508158	PFSK-1	brain:	n/a
35	chr11:64509084-64509134	T-47D	breast:	n/a
36	chr11:64511624-64511674	H1-hESC	embryonic stem cell:	embryo
37	chr11:64508421-64508471	ECC-1	luminal epithelium:	n/a
38	chr11:64512188-64512238	Hela-S3	cervix:	n/a
39	chr11:64509091-64509141	AG04449	skin:	fetal
40	chr11:64510466-64510516	BE2_C	brain:	n/a
41	chr11:64507260-64507310	PrEC	prostate:	n/a
42	chr11:64507260-64507310	SKMC	muscle:	n/a
43	chr11:64510112-64510162	AoSMC	blood vessel:	n/a
44	chr11:64509592-64509642	GM12892	blood:	n/a
45	chr11:64513809-64513859	K562	blood:	n/a
46	chr11:64510466-64510516	ECC-1	luminal epithelium:	n/a
47	chr11:64510466-64510516	Jurkat	blood:	n/a
48	chr11:64512197-64512247	SK-N-SH_RA	brain:	n/a
49	chr11:64511786-64511836	U87	brain:	n/a
50	chr11:64508509-64508559	HMEC	breast:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:64507790..64516181-chr11:64524582..64537783,30	K562	blood:
2	chr11:64511547..64513832-chr11:64538239..64542016,3	K562	blood:
3	chr11:64488142..64490863-chr11:64506214..64508875,2	MCF-7	breast:
4	chr11:64502299..64505841-chr11:64506050..64510563,6	K562	blood:
5	chr11:64502299..64505841-chr11:64506050..64510563,6	K562	blood:
6	chr11:64510149..64512039-chr11:64538219..64540894,2	MCF-7	breast:
7	chr10:70847451..70848345-chr11:64512509..64513406,2	NB4	blood:
8	chr11:64506030..64508610-chr11:64510560..64513523,3	MCF-7	breast:
9	chr11:64509463..64511820-chr11:64545145..64547148,2	MCF-7	breast:
10	chr11:64216411..64217094-chr11:64509920..64510560,2	K562	blood:
11	chr11:64510798..64511324-chr11:64535005..64535845,2	MCF-7	breast:
12	chr11:64420673..64421273-chr11:64510420..64510982,3	MCF-7	breast:
13	chr11:64509857..64513722-chr11:64571129..64574033,3	MCF-7	breast:
14	chr11:64510615..64511340-chr17:46047851..46048383,2	MCF-7	breast:
15	chr11:64506030..64508610-chr11:64510560..64513523,3	MCF-7	breast:
16	chr11:64489351..64492621-chr11:64507509..64512935,5	K562	blood:
17	chr11:64508515..64511238-chr11:64521497..64525046,4	MCF-7	breast:
18	chr11:64512574..64514468-chr11:64655571..64658129,2	K562	blood:
19	chr11:64491144..64492732-chr11:64505276..64507287,3	K562	blood:
20	chr11:64514464..64517911-chr11:64519413..64523331,4	MCF-7	breast:
21	chr11:64480253..64481992-chr11:64507131..64509338,2	K562	blood:
22	chr11:64512373..64514123-chr11:64641728..64643852,2	K562	blood:
23	chr11:64514464..64517911-chr11:64519413..64523331,4	MCF-7	breast:
24	chr11:64513308..64515346-chr11:64576654..64578254,2	K562	blood:
25	chr11:64503331..64505631-chr11:64505655..64508336,3	K562	blood:
26	chr11:64506827..64509728-chr11:64644773..64647136,2	K562	blood:
27	chr11:64503034..64505808-chr11:64508705..64511765,4	MCF-7	breast:
28	chr11:64490496..64491176-chr11:64510209..64510932,2	MCF-7	breast:
29	chr11:64489616..64492284-chr11:64509871..64511516,3	K562	blood:
30	chr11:64503034..64505808-chr11:64508705..64511765,4	MCF-7	breast:
31	chr11:64498850..64501502-chr11:64505614..64507569,2	K562	blood:
32	chr11:64510354..64515027-chr11:64543156..64548358,11	K562	blood:
33	chr11:64509047..64511433-chr11:64527648..64529214,2	MCF-7	breast:
34	chr11:64124497..64126994-chr11:64509396..64512374,2	K562	blood:
35	chr11:64509755..64511903-chr11:65684738..65686627,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PYGM-1	chr11:64509983-64510409	NONHSAT022014
2	lnc-PYGM-1	chr11:64512214-64512332	NONHSAT022014

No data

Variant related genes	Relation type
PYGM	TF binding region
RASGRP2	TF binding region
PYGM	CpG island
RASGRP2	CpG island
ENSG00000269038	chromatin interactions
ENSG00000181908	chromatin interactions
ENSG00000068976	chromatin interactions
ENSG00000175573	chromatin interactions
ENSG00000068831	chromatin interactions
ENSG00000122862	chromatin interactions
ENSG00000133895	chromatin interactions
ENSG00000108465	chromatin interactions
ENSG00000203400	chromatin interactions
ENSG00000110076	chromatin interactions
ENSG00000168066	chromatin interactions
ENSG00000162302	chromatin interactions
ENSG00000110047	chromatin interactions

Extended variants
information (count: 781 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2284301	chr11:64501991-64501992	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562856803	chr11:64502057-64502058	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376569818	chr11:64502095-64502096	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553737037	chr11:64502099-64502100	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531630297	chr11:64502148-64502149	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs551624746	chr11:64502166-64502167	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571642964	chr11:64502180-64502181	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77497097	chr11:64502198-64502199	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79717398	chr11:64502199-64502200	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs75659465	chr11:64502200-64502201	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs57558322	chr11:64502314-64502315	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs541140846	chr11:64502360-64502361	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs77537177	chr11:64502405-64502406	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547630944	chr11:64502504-64502505	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567238303	chr11:64502507-64502508	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs77004138	chr11:64502519-64502520	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183195599	chr11:64502538-64502539	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370805811	chr11:64502559-64502560	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150425817	chr11:64502595-64502596	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs373654113	chr11:64502608-64502609	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145230586	chr11:64502610-64502611	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs569602568	chr11:64502632-64502633	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371857837	chr11:64502633-64502634	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149091632	chr11:64502657-64502658	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375253063	chr11:64502661-64502662	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs144728511	chr11:64502676-64502677	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138764936	chr11:64502689-64502690	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs371237302	chr11:64502690-64502691	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538651164	chr11:64502712-64502713	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs374775399	chr11:64502715-64502716	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558873649	chr11:64502720-64502721	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200696134	chr11:64502724-64502725	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs116194408	chr11:64502754-64502755	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs554766114	chr11:64502755-64502756	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs117113441	chr11:64502774-64502775	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs141583891	chr11:64502775-64502776	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs371187689	chr11:64502817-64502818	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs545848701	chr11:64502844-64502845	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs71534256	chr11:64502846-64502847	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs75259448	chr11:64502874-64502875	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs528017609	chr11:64502916-64502917	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs191016351	chr11:64502939-64502940	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547693917	chr11:64502940-64502941	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs199801747	chr11:64502965-64502966	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs369856177	chr11:64503002-64503003	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs201703741	chr11:64503037-64503038	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201325045	chr11:64503040-64503041	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs141842144	chr11:64503043-64503044	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs145292489	chr11:64503044-64503045	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs538614428	chr11:64503059-64503060	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1253 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64491000-64502200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr11:64491200-64502200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr11:64491200-64502400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr11:64491200-64502800	Weak transcription	Gastric	stomach
5	chr11:64491400-64502200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr11:64491400-64503000	Weak transcription	Colon Smooth Muscle	Colon
7	chr11:64491400-64509400	Weak transcription	Right Atrium	heart
8	chr11:64491400-64509600	Weak transcription	Brain Angular Gyrus	brain
9	chr11:64491400-64509600	Weak transcription	Pancreas	Pancrea
10	chr11:64491600-64502600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:64491600-64503200	Weak transcription	Esophagus	oesophagus
12	chr11:64491600-64509200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:64491600-64509400	Weak transcription	Brain Hippocampus Middle	brain
14	chr11:64491800-64509400	Weak transcription	Brain Substantia Nigra	brain
15	chr11:64491800-64509800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:64492000-64509600	Weak transcription	Brain Cingulate Gyrus	brain
17	chr11:64493400-64502200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr11:64493400-64508800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:64493600-64502600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:64493600-64503800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:64493600-64507800	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr11:64493600-64508000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr11:64493800-64503600	Strong transcription	Primary B cells from peripheral blood	blood
24	chr11:64494000-64508400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr11:64494000-64508600	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr11:64494000-64508600	Strong transcription	Primary T cells from cord blood	blood
27	chr11:64494000-64508600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:64494200-64503400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr11:64494800-64503200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:64495800-64505200	Strong transcription	Fetal Thymus	thymus
31	chr11:64496600-64502200	Weak transcription	Lung	lung
32	chr11:64496600-64502400	Weak transcription	Aorta	Aorta
33	chr11:64497800-64504000	Weak transcription	Placenta	Placenta
34	chr11:64498000-64502200	Weak transcription	Liver	Liver
35	chr11:64498000-64502400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr11:64498000-64502400	Weak transcription	Right Ventricle	heart
37	chr11:64498000-64503800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:64498000-64503800	Strong transcription	Spleen	Spleen
39	chr11:64498000-64508400	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr11:64498200-64502200	Weak transcription	Adipose Nuclei	Adipose
41	chr11:64498200-64502600	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr11:64498200-64503200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:64498200-64509000	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr11:64498400-64506800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr11:64498400-64506800	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr11:64499400-64506800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr11:64499600-64502000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:64499600-64502200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
49	chr11:64499600-64502200	Weak transcription	Fetal Muscle Leg	muscle
50	chr11:64499600-64502400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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