Variant report

Variant	esv3344129
Chromosome Location	chr4:53524220-53527168
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:530)
CpG islands
(count:427)
Chromatin interactive
region (count:15)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:53524555-53524573	HepG2	liver:	n/a	n/a
2	ATF2	chr4:53523972-53524357	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr4:53525772-53526186	GM12878	blood:	n/a	chr4:53526160-53526173
4	BCLAF1	chr4:53525027-53525426	GM12878	blood:	n/a	chr4:53525404-53525417 chr4:53525409-53525422
5	BHLHE40	chr4:53525294-53525691	K562	blood:	n/a	n/a
6	BHLHE40	chr4:53525267-53526254	GM12878	blood:	n/a	chr4:53526096-53526112
7	CBX3	chr4:53525956-53526325	K562	blood:	n/a	n/a
8	CCNT2	chr4:53524913-53526337	K562	blood:	n/a	chr4:53525976-53525985 chr4:53524945-53524954
9	CEBPB	chr4:53523915-53524320	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:53523910-53524276	MCF-7	breast:	n/a	n/a
11	CEBPD	chr4:53525239-53525804	HepG2	liver:	n/a	n/a
12	CHD1	chr4:53526136-53526289	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD1	chr4:53525573-53525707	GM12878	blood:	n/a	n/a
14	CHD1	chr4:53525022-53525331	GM12878	blood:	n/a	n/a
15	CHD1	chr4:53525875-53525936	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr4:53525914-53526411	GM12878	blood:	n/a	chr4:53526060-53526070
17	CHD1	chr4:53524442-53524929	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr4:53525272-53526188	Hela-S3	cervix:	n/a	chr4:53526060-53526070
19	CHD2	chr4:53525926-53526024	HepG2	liver:	n/a	n/a
20	CHD2	chr4:53525376-53525558	HepG2	liver:	n/a	n/a
21	CHD2	chr4:53524733-53524812	K562	blood:	n/a	n/a
22	CHD2	chr4:53526145-53526440	GM12878	blood:	n/a	n/a
23	CHD2	chr4:53524089-53524414	HepG2	liver:	n/a	n/a
24	CHD2	chr4:53526267-53526445	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr4:53525252-53525799	K562	blood:	n/a	n/a
26	CHD2	chr4:53525682-53525703	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr4:53523955-53524309	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr4:53524896-53525793	GM12878	blood:	n/a	n/a
29	CREB1	chr4:53525465-53525782	A549	lung:	n/a	n/a
30	CTBP2	chr4:53523874-53524645	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr4:53524080-53524230	HMF	breast:	n/a	n/a
32	CTCF	chr4:53524100-53524250	AG10803	skin:	n/a	n/a
33	CTCF	chr4:53526080-53526230	GM06990	blood:	n/a	chr4:53526095-53526108
34	CTCF	chr4:53526181-53526209	GM10266	blood:	n/a	n/a
35	CTCF	chr4:53524840-53524990	AG04449	skin:	n/a	n/a
36	CTCF	chr4:53524960-53525110	AG04449	skin:	n/a	n/a
37	CTCF	chr4:53525326-53525411	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:53525220-53525370	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr4:53526020-53526170	HMEC	breast:	n/a	chr4:53526095-53526108 chr4:53526024-53526034
40	CTCF	chr4:53524260-53524410	GM06990	blood:	n/a	n/a
41	CTCF	chr4:53524100-53524250	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr4:53524160-53524310	BJ	skin:	n/a	n/a
43	CTCF	chr4:53524140-53524290	AoAF	blood vessel:	n/a	n/a
44	CTCF	chr4:53524100-53524250	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr4:53524340-53524490	AG04449	skin:	n/a	n/a
46	CTCF	chr4:53526169-53526254	GM19238	blood:	n/a	n/a
47	CTCF	chr4:53526000-53526150	HCPEpiC	choroid plexus:	n/a	chr4:53526095-53526108 chr4:53526024-53526034 chr4:53526019-53526037
48	CTCF	chr4:53525262-53525385	GM12892	blood:	n/a	n/a
49	CTCF	chr4:53526131-53526179	GM12891	blood:	n/a	n/a
50	CTCF	chr4:53526080-53526347	GM12878	blood:	n/a	chr4:53526095-53526108

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:53526629-53526679	SK-N-MC	brain:	n/a
2	chr4:53525745-53525795	HEEpiC	esophagus:	n/a
3	chr4:53524296-53524346	SKMC	muscle:	n/a
4	chr4:53525271-53525321	BJ	skin:	n/a
5	chr4:53526629-53526679	HCPEpiC	choroid plexus:	n/a
6	chr4:53526226-53526276	ovcar-3	ovarian:	n/a
7	chr4:53525403-53525453	HMEC	breast:	n/a
8	chr4:53526629-53526679	HCM	heart:	n/a
9	chr4:53525715-53525765	HMEC	breast:	n/a
10	chr4:53525403-53525453	HIPEpiC	eye:	n/a
11	chr4:53525745-53525795	RPTEC	kidney:	n/a
12	chr4:53525271-53525321	IMR90	lung:	fetal
13	chr4:53525715-53525765	RPTEC	kidney:	n/a
14	chr4:53525403-53525453	NHDF-neo	bronchial:	n/a
15	chr4:53525403-53525453	PANC-1	pancreas:	n/a
16	chr4:53524296-53524346	HCT-116	colon:	n/a
17	chr4:53525715-53525765	BE2_C	brain:	n/a
18	chr4:53526629-53526679	BE2_C	brain:	n/a
19	chr4:53525715-53525765	NT2-D1	testis:	n/a
20	chr4:53525271-53525321	NHBE	bronchial:	n/a
21	chr4:53526226-53526276	GM12892	blood:	n/a
22	chr4:53524296-53524346	HEK293	kidney:	embryo
23	chr4:53525745-53525795	K562	blood:	n/a
24	chr4:53526629-53526679	Caco-2	colon:	n/a
25	chr4:53524296-53524346	HRPEpiC	eye:	n/a
26	chr4:53525403-53525453	T-47D	breast:	n/a
27	chr4:53525745-53525795	HCF	heart:	n/a
28	chr4:53525745-53525795	IMR90	lung:	fetal
29	chr4:53525403-53525453	BJ	skin:	n/a
30	chr4:53526629-53526679	ovcar-3	ovarian:	n/a
31	chr4:53524296-53524346	Caco-2	colon:	n/a
32	chr4:53525403-53525453	Hepatocyte	liver:	n/a
33	chr4:53525271-53525321	NHDF-neo	bronchial:	n/a
34	chr4:53526226-53526276	HNPCEpiC	eye:	n/a
35	chr4:53525403-53525453	NT2-D1	testis:	n/a
36	chr4:53525745-53525795	HIPEpiC	eye:	n/a
37	chr4:53525745-53525795	U87	brain:	n/a
38	chr4:53526226-53526276	HUVEC	blood vessel:	n/a
39	chr4:53526226-53526276	NHDF-neo	bronchial:	n/a
40	chr4:53526629-53526679	AG09309	skin:	n/a
41	chr4:53525715-53525765	HEEpiC	esophagus:	n/a
42	chr4:53526629-53526679	HEK293	kidney:	embryo
43	chr4:53526629-53526679	AG09319	gingival:	n/a
44	chr4:53526629-53526679	LNCaP	prostate:	n/a
45	chr4:53526226-53526276	SKMC	muscle:	n/a
46	chr4:53526226-53526276	MCF-7	breast:	n/a
47	chr4:53526226-53526276	HPAEpiC	pulmonary alveolar:	n/a
48	chr4:53525271-53525321	HCT-116	colon:	n/a
49	chr4:53526226-53526276	AG09319	gingival:	n/a
50	chr4:53525403-53525453	AG10803	skin:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:53524001..53527558-chr4:53577308..53580194,4	MCF-7	breast:
2	chr4:53525628..53527969-chr4:53583632..53585496,2	MCF-7	breast:
3	chr4:53525430..53527688-chr4:53726700..53729187,4	MCF-7	breast:
4	chr4:53526307..53527847-chr4:53553354..53555429,2	MCF-7	breast:
5	chr4:53522789..53525024-chr4:53586830..53589438,2	K562	blood:
6	chr17:5389478..5390355-chr4:53525501..53526123,2	Hela-S3	cervix:
7	chr4:53526174..53528019-chr4:53536016..53537973,2	K562	blood:
8	chr4:53523968..53528771-chr4:53576572..53580241,9	MCF-7	breast:
9	chr4:53519355..53522911-chr4:53523707..53526726,6	MCF-7	breast:
10	chr4:53515781..53522890-chr4:53523068..53527068,15	MCF-7	breast:
11	chr4:53522503..53529252-chr4:53576629..53581800,10	K562	blood:
12	chr4:53455945..53458250-chr4:53525790..53527663,3	K562	blood:
13	chr4:53523914..53526614-chr4:53586643..53588754,3	MCF-7	breast:
14	chr4:53492777..53495734-chr4:53523846..53526517,2	K562	blood:
15	chr4:53523849..53530507-chr4:53576531..53584814,17	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASL11B-5	chr4:53527059-53532526	NONHSAT096366
2	lnc-RASL11B-5	chr4:53525573-53525843	ENSG00000248866.1
3	lnc-RASL11B-5	chr4:53527059-53527325	NONHSAT096365
4	lnc-RASL11B-5	chr4:53527059-53527835	ENSG00000248866.1
5	lnc-RASL11B-5	chr4:53525597-53525843	NONHSAT096366

No data

Variant related genes	Relation type
USP46	TF binding region
USP46-AS1	TF binding region
USP46	CpG island
USP46-AS1	CpG island
ENSG00000128045	chromatin interactions
ENSG00000109189	chromatin interactions
ENSG00000264585	chromatin interactions
ENSG00000248375	chromatin interactions
ENSG00000226950	chromatin interactions
ENSG00000167842	chromatin interactions
ENSG00000072849	chromatin interactions
ENSG00000212588	chromatin interactions

Extended variants
information (count: 85 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531409553	chr4:53524251-53524252	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs572859143	chr4:53524287-53524288	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs548659666	chr4:53524311-53524312	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs4311371	chr4:53524319-53524320	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs60268144	chr4:53524352-53524353	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs568501521	chr4:53524370-53524371	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs534181911	chr4:53524386-53524387	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs547837951	chr4:53524445-53524446	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs115119057	chr4:53524451-53524452	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs149803595	chr4:53524471-53524472	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs34485888	chr4:53524568-53524569	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs556902263	chr4:53524570-53524571	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs576536186	chr4:53524591-53524592	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs375284592	chr4:53524596-53524597	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs58964773	chr4:53524605-53524606	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs554642261	chr4:53524670-53524671	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs574484193	chr4:53524702-53524703	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs539821025	chr4:53524734-53524735	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs377495564	chr4:53524761-53524762	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs559691150	chr4:53524809-53524810	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs181557943	chr4:53524817-53524818	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs545645718	chr4:53524824-53524825	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs184675098	chr4:53524842-53524843	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs562488900	chr4:53524906-53524907	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs28430452	chr4:53524939-53524940	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs375509202	chr4:53524951-53524952	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs562188173	chr4:53525023-53525024	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs527754134	chr4:53525052-53525053	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs547923974	chr4:53525077-53525078	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs375877717	chr4:53525146-53525147	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs368313441	chr4:53525147-53525148	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs547018072	chr4:53525153-53525154	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs79002691	chr4:53525171-53525172	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs536033789	chr4:53525191-53525192	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs76840131	chr4:53525221-53525222	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs572623224	chr4:53525242-53525243	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs374323887	chr4:53525347-53525348	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs377293826	chr4:53525360-53525361	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs533608665	chr4:53525375-53525376	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs553460550	chr4:53525394-53525395	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs576426860	chr4:53525400-53525401	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs545433987	chr4:53525432-53525433	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs556406760	chr4:53525471-53525472	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs576285443	chr4:53525498-53525499	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs565017100	chr4:53525514-53525515	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs542127326	chr4:53525557-53525558	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs561694750	chr4:53525585-53525586	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
48	rs527489621	chr4:53525707-53525708	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
49	rs541487949	chr4:53525711-53525712	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
50	rs564619996	chr4:53525907-53525908	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioblastoma multiforme	21569311	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:53510800-53524400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:53511600-53524600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:53512000-53524400	Weak transcription	Primary B cells from cord blood	blood
4	chr4:53513800-53524600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr4:53518600-53525200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr4:53518800-53524600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr4:53521400-53524400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:53522800-53524400	Enhancers	Lung	lung
9	chr4:53523000-53527000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:53523200-53524400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:53523600-53524600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr4:53523600-53524600	Flanking Active TSS	Brain Germinal Matrix	brain
13	chr4:53523600-53524600	Enhancers	Psoas Muscle	Psoas
14	chr4:53523600-53524800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr4:53523600-53524800	Enhancers	Primary B cells from peripheral blood	blood
16	chr4:53523600-53524800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr4:53523600-53524800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:53523600-53524800	Flanking Active TSS	Right Ventricle	heart
19	chr4:53523600-53524800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr4:53523600-53524800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
21	chr4:53523600-53525000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
22	chr4:53523600-53526400	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr4:53523800-53524400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:53523800-53524400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:53523800-53524400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr4:53523800-53524400	Enhancers	Liver	Liver
27	chr4:53523800-53524400	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr4:53523800-53524600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr4:53523800-53524600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:53523800-53524600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr4:53523800-53524600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr4:53523800-53524600	Flanking Active TSS	Esophagus	oesophagus
33	chr4:53523800-53524600	Flanking Active TSS	Fetal Stomach	stomach
34	chr4:53523800-53524600	Flanking Active TSS	Ovary	ovary
35	chr4:53523800-53524600	Flanking Active TSS	HMEC	breast
36	chr4:53523800-53524800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr4:53523800-53524800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr4:53523800-53524800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr4:53523800-53524800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr4:53523800-53524800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr4:53523800-53524800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:53523800-53524800	Flanking Active TSS	Brain Anterior Caudate	brain
43	chr4:53523800-53524800	Flanking Active TSS	Fetal Brain Female	brain
44	chr4:53523800-53524800	Flanking Active TSS	Fetal Muscle Trunk	muscle
45	chr4:53523800-53524800	Flanking Active TSS	Left Ventricle	heart
46	chr4:53523800-53525000	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr4:53523800-53525000	Flanking Active TSS	Fetal Muscle Leg	muscle
48	chr4:53523800-53525000	Flanking Active TSS	HepG2	liver
49	chr4:53523800-53526200	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr4:53523800-53526400	Active TSS	Brain Angular Gyrus	brain

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