Variant report

Variant	esv3325631
Chromosome Location	chr4:110354028-110356876
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:110354211-110354931	HepG2	liver:	n/a	n/a
2	ATF2	chr4:110354473-110355010	GM12878	blood:	n/a	n/a
3	ATF3	chr4:110354590-110355029	K562	blood:	n/a	n/a
4	ATF3	chr4:110354491-110354811	A549	lung:	n/a	n/a
5	BACH1	chr4:110355512-110355621	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:110354710-110354946	K562	blood:	n/a	n/a
7	BACH1	chr4:110354432-110355016	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr4:110354481-110355062	GM12878	blood:	n/a	chr4:110354645-110354658 chr4:110354725-110354738 chr4:110354752-110354765
9	BCLAF1	chr4:110354396-110355310	GM12878	blood:	n/a	chr4:110354645-110354658 chr4:110354725-110354738 chr4:110354752-110354765
10	BHLHE40	chr4:110355440-110355810	HepG2	liver:	n/a	n/a
11	BHLHE40	chr4:110354543-110355029	GM12878	blood:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
12	BHLHE40	chr4:110355604-110356009	K562	blood:	n/a	chr4:110355801-110355817
13	BHLHE40	chr4:110355545-110356014	GM12878	blood:	n/a	chr4:110355801-110355817
14	BHLHE40	chr4:110354469-110355120	HepG2	liver:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
15	BHLHE40	chr4:110354288-110355032	K562	blood:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
16	BHLHE40	chr4:110354627-110354827	A549	lung:	n/a	chr4:110354719-110354735 chr4:110354642-110354658 chr4:110354645-110354661
17	BRCA1	chr4:110354583-110354804	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr4:110354768-110354947	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:110354689-110354889	HepG2	liver:	n/a	n/a
20	CBX3	chr4:110354275-110355033	K562	blood:	n/a	n/a
21	CCNT2	chr4:110354501-110355331	K562	blood:	n/a	n/a
22	CEBPB	chr4:110356704-110357250	HepG2	liver:	n/a	chr4:110356879-110356890 chr4:110356986-110356998
23	CEBPB	chr4:110356841-110357027	K562	blood:	n/a	chr4:110356879-110356890 chr4:110356986-110356998
24	CEBPB	chr4:110354600-110354908	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:110353478-110354091	A549	lung:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
26	CEBPB	chr4:110353435-110354161	IMR90	lung:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
27	CEBPB	chr4:110353519-110354064	K562	blood:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
28	CEBPB	chr4:110353476-110354386	Hela-S3	cervix:	n/a	chr4:110353616-110353627 chr4:110353617-110353628 chr4:110353616-110353629 chr4:110353618-110353627 chr4:110353881-110353892
29	CEBPB	chr4:110356777-110357165	HepG2	liver:	n/a	chr4:110356879-110356890 chr4:110356986-110356998
30	CEBPB	chr4:110356710-110357075	IMR90	lung:	n/a	chr4:110356879-110356890 chr4:110356986-110356998
31	CEBPB	chr4:110354588-110355000	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:110356707-110357099	Hela-S3	cervix:	n/a	chr4:110356879-110356890 chr4:110356986-110356998
33	CEBPB	chr4:110356770-110357072	A549	lung:	n/a	chr4:110356879-110356890 chr4:110356986-110356998
34	CEBPB	chr4:110356813-110357085	HepG2	liver:	n/a	chr4:110356879-110356890 chr4:110356986-110356998
35	CEBPD	chr4:110354505-110355207	HepG2	liver:	n/a	n/a
36	CHD1	chr4:110354529-110354915	GM12878	blood:	n/a	n/a
37	CHD1	chr4:110355474-110355809	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr4:110354216-110354720	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr4:110354399-110355043	GM12878	blood:	n/a	n/a
40	CHD2	chr4:110354323-110355067	HepG2	liver:	n/a	n/a
41	CHD2	chr4:110354553-110355068	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr4:110354495-110354992	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr4:110354486-110354971	K562	blood:	n/a	n/a
44	CHD2	chr4:110355466-110355836	GM12878	blood:	n/a	n/a
45	CREB1	chr4:110354509-110355241	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr4:110354551-110355299	A549	lung:	n/a	n/a
47	CREB1	chr4:110354488-110355154	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr4:110354409-110355456	HepG2	liver:	n/a	n/a
49	CREB1	chr4:110354429-110355267	HepG2	liver:	n/a	n/a
50	CREB1	chr4:110354544-110355262	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:110354896-110354946	Hepatocyte	liver:	n/a
2	chr4:110354896-110354946	Jurkat	blood:	n/a
3	chr4:110354896-110354946	Hepatocyte	liver:	n/a
4	chr4:110354896-110354946	Jurkat	blood:	n/a
5	chr4:110355472-110355522	HMEC	breast:	n/a
6	chr4:110354443-110354493	AG04449	skin:	fetal
7	chr4:110355447-110355497	AoSMC	blood vessel:	n/a
8	chr4:110355525-110355575	SK-N-MC	brain:	n/a
9	chr4:110355447-110355497	SKMC	muscle:	n/a
10	chr4:110355472-110355522	NB4	blood:	n/a
11	chr4:110354674-110354724	K562	blood:	n/a
12	chr4:110354443-110354493	Hela-S3	cervix:	n/a
13	chr4:110354896-110354946	MCF10A-Er-Src	breast:	n/a
14	chr4:110354443-110354493	MCF10A-Er-Src	breast:	n/a
15	chr4:110355680-110355730	Hepatocyte	liver:	n/a
16	chr4:110354443-110354493	HEEpiC	esophagus:	n/a
17	chr4:110354820-110354870	GM12878	blood:	n/a
18	chr4:110354443-110354493	NHBE	bronchial:	n/a
19	chr4:110355447-110355497	Jurkat	blood:	n/a
20	chr4:110355680-110355730	HRPEpiC	eye:	n/a
21	chr4:110355447-110355497	GM12892	blood:	n/a
22	chr4:110355680-110355730	HCM	heart:	n/a
23	chr4:110355525-110355575	PANC-1	pancreas:	n/a
24	chr4:110355680-110355730	MCF10A-Er-Src	breast:	n/a
25	chr4:110355472-110355522	HepG2	liver:	n/a
26	chr4:110355472-110355522	ProgFib	skin:	n/a
27	chr4:110354443-110354493	AG09309	skin:	n/a
28	chr4:110354443-110354493	GM12892	blood:	n/a
29	chr4:110354354-110354404	NH-A	brain:	n/a
30	chr4:110354923-110354973	HMEC	breast:	n/a
31	chr4:110354820-110354870	HCM	heart:	n/a
32	chr4:110354896-110354946	HRPEpiC	eye:	n/a
33	chr4:110354354-110354404	AG04450	lung:	fetal
34	chr4:110355447-110355497	Caco-2	colon:	n/a
35	chr4:110354354-110354404	HMEC	breast:	n/a
36	chr4:110355680-110355730	NT2-D1	testis:	n/a
37	chr4:110354674-110354724	ovcar-3	ovarian:	n/a
38	chr4:110354674-110354724	HL-60	blood:	n/a
39	chr4:110354923-110354973	HCM	heart:	n/a
40	chr4:110355472-110355522	H1-hESC	embryonic stem cell:	embryo
41	chr4:110355680-110355730	HCT-116	colon:	n/a
42	chr4:110354896-110354946	HCF	heart:	n/a
43	chr4:110355680-110355730	AG10803	skin:	n/a
44	chr4:110354820-110354870	AG09319	gingival:	n/a
45	chr4:110354674-110354724	CMK	blood:	n/a
46	chr4:110355472-110355522	CMK	blood:	n/a
47	chr4:110354923-110354973	GM12891	blood:	n/a
48	chr4:110354820-110354870	U87	brain:	n/a
49	chr4:110355525-110355575	Jurkat	blood:	n/a
50	chr4:110355447-110355497	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:109540362..109542277-chr4:110353620..110356489,2	K562	blood:
2	chr14:105261712..105263242-chr4:110355266..110356786,2	MCF-7	breast:
3	chr4:110353826..110356085-chr4:110735938..110738635,3	MCF-7	breast:
4	chr4:110353323..110356452-chr4:110478874..110481567,4	MCF-7	breast:
5	chr4:110351870..110353542-chr4:110355047..110357946,2	MCF-7	breast:
6	chr4:110351897..110354482-chr4:110431012..110433361,3	MCF-7	breast:
7	chr4:109542488..109544674-chr4:110355892..110357950,2	K562	blood:
8	chr4:110354680..110356371-chr4:110650734..110652526,2	MCF-7	breast:
9	chr4:110354421..110354923-chr7:44084218..44084744,2	Hela-S3	cervix:
10	chr4:110353269..110354820-chr4:110577196..110580148,2	MCF-7	breast:
11	chr4:110352891..110355275-chr4:110649929..110651520,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL25A1-1	chr4:110354890-110354920	ENSG00000247950
2	lnc-COL25A1-1	chr4:110354890-110354973	ENSG00000247950
3	lnc-COL25A1-1	chr4:110354890-110354939	ENSG00000247950

Variant related genes	Relation type
SEC24B-AS1	TF binding region
SEC24B	TF binding region
SEC24B-AS1	CpG island
SEC24B	CpG island
ENSG00000109475	chromatin interactions
ENSG00000005059	chromatin interactions
ENSG00000272795	chromatin interactions
ENSG00000109534	chromatin interactions
ENSG00000123739	chromatin interactions
ENSG00000136279	chromatin interactions
ENSG00000142208	chromatin interactions
ENSG00000234492	chromatin interactions
CCNG1	miRNA target sites
ATP6V1C1	miRNA target sites
G3BP1	miRNA target sites

Extended variants
information (count: 80 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536562613	chr4:110354028-110354029	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs371908545	chr4:110354042-110354043	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs10016533	chr4:110354054-110354055	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs78124433	chr4:110354074-110354075	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs558389948	chr4:110354079-110354080	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs538650531	chr4:110354083-110354084	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs558873936	chr4:110354103-110354104	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs575655606	chr4:110354126-110354127	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs373347063	chr4:110354131-110354132	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs7375900	chr4:110354155-110354156	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs11369038	chr4:110354157-110354158	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs397705042	chr4:110354174-110354175	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs551790691	chr4:110354187-110354188	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs544691662	chr4:110354252-110354253	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs576471352	chr4:110354280-110354281	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs151143846	chr4:110354418-110354419	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs540622048	chr4:110354433-110354434	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs77326245	chr4:110354456-110354457	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs189459377	chr4:110354492-110354493	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs560185560	chr4:110354493-110354494	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs532173387	chr4:110354538-110354539	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs79665044	chr4:110354557-110354558	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs562456698	chr4:110354593-110354594	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs531326472	chr4:110354632-110354633	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs76023249	chr4:110354682-110354683	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs567551528	chr4:110354721-110354722	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs536423717	chr4:110354739-110354740	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs180697394	chr4:110354790-110354791	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs567063509	chr4:110354793-110354794	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs185054241	chr4:110354819-110354820	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs371131199	chr4:110354821-110354822	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs534049793	chr4:110354873-110354874	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs71603023	chr4:110354889-110354890	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs575677521	chr4:110354899-110354900	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
35	rs538377411	chr4:110354966-110354967	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
36	rs72896632	chr4:110354973-110354974	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs570129880	chr4:110355097-110355098	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs574733736	chr4:110355129-110355130	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs540044361	chr4:110355136-110355137	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs553890452	chr4:110355176-110355177	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs577065985	chr4:110355305-110355306	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs13103419	chr4:110355351-110355352	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs546049130	chr4:110355410-110355411	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs115096670	chr4:110355463-110355464	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs531190289	chr4:110355486-110355487	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs541550304	chr4:110355493-110355494	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs190301923	chr4:110355546-110355547	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs527347571	chr4:110355553-110355554	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs546883957	chr4:110355582-110355583	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs181123724	chr4:110355750-110355751	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Oral squamous cell carcinoma	17134496	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Schizophrenia	19546859	CNVD
Colorectal cancer	16272173	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110345200-110354200	Weak transcription	Ovary	ovary
2	chr4:110346000-110354400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:110351000-110354400	Weak transcription	Pancreas	Pancrea
4	chr4:110353200-110354200	Enhancers	Fetal Heart	heart
5	chr4:110353200-110354200	Flanking Active TSS	Fetal Kidney	kidney
6	chr4:110353400-110354200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:110353400-110354200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr4:110353400-110354200	Weak transcription	Psoas Muscle	Psoas
9	chr4:110353400-110354400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
10	chr4:110353400-110354600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:110353400-110356600	Active TSS	K562	blood
12	chr4:110353600-110354200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr4:110353600-110354200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr4:110353600-110354200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr4:110353600-110354200	Flanking Active TSS	Fetal Intestine Small	intestine
16	chr4:110353600-110354200	Flanking Active TSS	Fetal Lung	lung
17	chr4:110353600-110354200	Enhancers	Placenta	Placenta
18	chr4:110353600-110354200	Enhancers	Placenta Amnion	Placenta Amnion
19	chr4:110353600-110354200	Enhancers	Small Intestine	intestine
20	chr4:110353600-110354200	Flanking Active TSS	NHEK	skin
21	chr4:110353600-110354400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr4:110353600-110354400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
23	chr4:110353600-110354400	Flanking Active TSS	Brain Hippocampus Middle	brain
24	chr4:110353600-110354600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr4:110353600-110354600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:110353600-110354600	Flanking Active TSS	HUVEC	blood vessel
27	chr4:110353600-110354600	Flanking Active TSS	Osteobl	bone
28	chr4:110353600-110354800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr4:110353600-110357000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr4:110353800-110354200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr4:110353800-110354200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr4:110353800-110354200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:110353800-110354200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr4:110353800-110354200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr4:110353800-110354200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr4:110353800-110354200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
37	chr4:110353800-110354200	Flanking Active TSS	Brain Angular Gyrus	brain
38	chr4:110353800-110354200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr4:110353800-110354200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr4:110353800-110354200	Flanking Active TSS	Fetal Muscle Leg	muscle
41	chr4:110353800-110354400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr4:110353800-110354400	Flanking Active TSS	Primary T cells from cord blood	blood
43	chr4:110353800-110354400	Flanking Active TSS	Primary hematopoietic stem cells	blood
44	chr4:110353800-110354400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
45	chr4:110353800-110354400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr4:110353800-110354400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr4:110353800-110354400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr4:110353800-110354400	Flanking Active TSS	Liver	Liver
49	chr4:110353800-110354400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr4:110353800-110354400	Flanking Active TSS	Colon Smooth Muscle	Colon

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