Variant report

Variant	nsv878534
Chromosome Location	chr4:7084985-7121880
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:716)
CpG islands
(count:673)
Chromatin interactive
region (count:40)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:7105314-7105465	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr4:7092294-7092560	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:7105183-7105776	HepG2	liver:	n/a	n/a
4	BHLHE40	chr4:7107217-7107412	K562	blood:	n/a	n/a
5	BHLHE40	chr4:7103743-7104167	K562	blood:	n/a	n/a
6	BHLHE40	chr4:7104815-7104956	K562	blood:	n/a	n/a
7	BHLHE40	chr4:7103753-7104166	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:7105336-7105646	K562	blood:	n/a	n/a
9	BRCA1	chr4:7105407-7105588	HepG2	liver:	n/a	n/a
10	BRCA1	chr4:7105871-7105910	HepG2	liver:	n/a	n/a
11	CBX3	chr4:7088056-7088466	K562	blood:	n/a	n/a
12	CBX3	chr4:7088047-7088408	K562	blood:	n/a	n/a
13	CCNT2	chr4:7104691-7105294	K562	blood:	n/a	n/a
14	CEBPB	chr4:7095986-7096192	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:7096011-7096198	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:7108227-7108494	HepG2	liver:	n/a	chr4:7108367-7108378
17	CEBPB	chr4:7108245-7108467	IMR90	lung:	n/a	chr4:7108367-7108378
18	CEBPB	chr4:7108265-7108459	K562	blood:	n/a	chr4:7108367-7108378
19	CEBPD	chr4:7104915-7105175	HepG2	liver:	n/a	n/a
20	CEBPD	chr4:7103881-7104207	HepG2	liver:	n/a	n/a
21	CHD2	chr4:7104986-7105031	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr4:7105020-7105542	HepG2	liver:	n/a	n/a
23	CHD2	chr4:7104819-7105480	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr4:7104789-7104974	K562	blood:	n/a	n/a
25	CREB1	chr4:7104884-7105175	A549	lung:	n/a	n/a
26	CTCF	chr4:7104740-7104890	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr4:7104640-7104790	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr4:7104840-7104990	AG09319	gingival:	n/a	n/a
29	CTCF	chr4:7103820-7103970	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr4:7103778-7104031	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:7103880-7104030	GM12878	blood:	n/a	n/a
32	CTCF	chr4:7103800-7103950	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr4:7103749-7104068	GM19239	blood:	n/a	n/a
34	CTCF	chr4:7088840-7088990	GM06990	blood:	n/a	n/a
35	CTCF	chr4:7104791-7104798	K562	blood:	n/a	n/a
36	CTCF	chr4:7103756-7104051	Gliobla	brain:	n/a	n/a
37	CTCF	chr4:7103860-7104010	GM12871	blood:	n/a	n/a
38	CTCF	chr4:7103860-7104010	SAEC	small airway:	n/a	n/a
39	CTCF	chr4:7103820-7103970	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr4:7103820-7103970	AG04450	lung:	n/a	n/a
41	CTCF	chr4:7104640-7104790	GM12867	blood:	n/a	n/a
42	CTCF	chr4:7104720-7104870	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr4:7103860-7104010	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr4:7103840-7103990	GM12864	blood:	n/a	n/a
45	CTCF	chr4:7104839-7104868	LNCaP	prostate:	n/a	n/a
46	CTCF	chr4:7103880-7104030	Caco-2	colon:	n/a	n/a
47	CTCF	chr4:7103761-7104019	Lung_OC	lung:	n/a	n/a
48	CTCF	chr4:7104749-7104940	GM12892	blood:	n/a	n/a
49	CTCF	chr4:7103880-7104030	A549	lung:	n/a	n/a
50	CTCF	chr4:7103820-7103970	AoAF	blood vessel:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7105262-7105312	ECC-1	luminal epithelium:	n/a
2	chr4:7106195-7106245	NT2-D1	testis:	n/a
3	chr4:7105262-7105312	ECC-1	luminal epithelium:	n/a
4	chr4:7106195-7106245	NT2-D1	testis:	n/a
5	chr4:7105115-7105165	HEEpiC	esophagus:	n/a
6	chr4:7105573-7105623	RPTEC	kidney:	n/a
7	chr4:7114046-7114096	IMR90	lung:	fetal
8	chr4:7105115-7105165	PFSK-1	brain:	n/a
9	chr4:7105272-7105322	HNPCEpiC	eye:	n/a
10	chr4:7104897-7104947	HIPEpiC	eye:	n/a
11	chr4:7105262-7105312	HCF	heart:	n/a
12	chr4:7114012-7114062	GM12892	blood:	n/a
13	chr4:7114046-7114096	MCF-7	breast:	n/a
14	chr4:7114067-7114117	HRPEpiC	eye:	n/a
15	chr4:7105262-7105312	NB4	blood:	n/a
16	chr4:7104195-7104245	NB4	blood:	n/a
17	chr4:7114012-7114062	HepG2	liver:	n/a
18	chr4:7114046-7114096	AG09309	skin:	n/a
19	chr4:7106195-7106245	A549	lung:	n/a
20	chr4:7105115-7105165	U87	brain:	n/a
21	chr4:7105573-7105623	A549	lung:	n/a
22	chr4:7114046-7114096	HUVEC	blood vessel:	n/a
23	chr4:7106195-7106245	T-47D	breast:	n/a
24	chr4:7114067-7114117	PrEC	prostate:	n/a
25	chr4:7114046-7114096	GM19239	blood:	n/a
26	chr4:7105262-7105312	MCF-7	breast:	n/a
27	chr4:7104897-7104947	HCPEpiC	choroid plexus:	n/a
28	chr4:7106195-7106245	AG04449	skin:	fetal
29	chr4:7114046-7114096	Hela-S3	cervix:	n/a
30	chr4:7105262-7105312	ProgFib	skin:	n/a
31	chr4:7104195-7104245	K562	blood:	n/a
32	chr4:7106023-7106073	HIPEpiC	eye:	n/a
33	chr4:7114046-7114096	HRCEpiC	kidney:	n/a
34	chr4:7114012-7114062	NH-A	brain:	n/a
35	chr4:7104195-7104245	AG04450	lung:	fetal
36	chr4:7104897-7104947	HCF	heart:	n/a
37	chr4:7106195-7106245	SKMC	muscle:	n/a
38	chr4:7105262-7105312	ovcar-3	ovarian:	n/a
39	chr4:7105115-7105165	GM12891	blood:	n/a
40	chr4:7105272-7105322	SK-N-MC	brain:	n/a
41	chr4:7106023-7106073	CMK	blood:	n/a
42	chr4:7105573-7105623	AG04449	skin:	fetal
43	chr4:7105115-7105165	GM12892	blood:	n/a
44	chr4:7114012-7114062	IMR90	lung:	fetal
45	chr4:7105272-7105322	BE2_C	brain:	n/a
46	chr4:7105272-7105322	HUVEC	blood vessel:	n/a
47	chr4:7105272-7105322	SK-N-SH_RA	brain:	n/a
48	chr4:7105272-7105322	ECC-1	luminal epithelium:	n/a
49	chr4:7114012-7114062	ProgFib	skin:	n/a
50	chr4:7104195-7104245	AG04449	skin:	fetal

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7097658..7100396-chr4:7102280..7105139,5	K562	blood:
2	chr4:7114517..7116267-chr4:7117721..7119678,2	K562	blood:
3	chr4:7086060..7087996-chr4:7103709..7106625,2	K562	blood:
4	chr4:7103774..7104291-chr4:7158329..7158835,2	MCF-7	breast:
5	chr4:7088413..7090570-chr4:7093679..7095355,2	K562	blood:
6	chr4:7083980..7086191-chr4:7094533..7096477,2	K562	blood:
7	chr4:7096598..7098168-chr4:7102324..7105190,2	MCF-7	breast:
8	chr4:7088413..7090570-chr4:7093679..7095355,2	K562	blood:
9	chr4:7105809..7107677-chr4:7109830..7111435,2	K562	blood:
10	chr4:7103913..7106622-chr4:7111535..7115141,3	K562	blood:
11	chr4:7120740..7122988-chr4:7129086..7130661,2	MCF-7	breast:
12	chr4:7083964..7086960-chr4:7088708..7091240,2	K562	blood:
13	chr4:7077408..7080531-chr4:7105216..7108085,3	K562	blood:
14	chr4:7103913..7105517-chr4:7112314..7115141,2	K562	blood:
15	chr4:7115313..7118277-chr4:7121147..7123527,2	MCF-7	breast:
16	chr4:7114517..7116267-chr4:7117721..7119678,2	K562	blood:
17	chr4:7083964..7086960-chr4:7088708..7091240,2	K562	blood:
18	chr4:7098558..7101540-chr4:7102623..7104219,2	MCF-7	breast:
19	chr4:7121664..7124511-chr4:7134767..7137572,2	K562	blood:
20	chr4:7067941..7072292-chr4:7099619..7103393,4	MCF-7	breast:
21	chr4:7105423..7108283-chr4:7118442..7120103,2	MCF-7	breast:
22	chr4:7105147..7106911-chr4:7141540..7143652,2	K562	blood:
23	chr4:7106689..7108245-chr4:7109405..7112071,2	MCF-7	breast:
24	chr4:7043790..7046279-chr4:7102506..7105292,2	K562	blood:
25	chr4:7093602..7095834-chr4:7100410..7102327,2	MCF-7	breast:
26	chr4:7103913..7105517-chr4:7112314..7115141,2	K562	blood:
27	chr4:7098558..7101540-chr4:7102623..7104219,2	MCF-7	breast:
28	chr4:7099425..7101930-chr4:7102267..7105259,4	MCF-7	breast:
29	chr4:7096026..7100396-chr4:7102325..7105652,7	K562	blood:
30	chr4:7103610..7105955-chr4:7121635..7124295,2	K562	blood:
31	chr4:7093602..7095834-chr4:7100410..7102327,2	MCF-7	breast:
32	chr4:7083980..7086191-chr4:7094533..7096477,2	K562	blood:
33	chr4:7103913..7106622-chr4:7111535..7115141,3	K562	blood:
34	chr4:7105809..7107677-chr4:7109830..7111435,2	K562	blood:
35	chr4:7106689..7108245-chr4:7109405..7112071,2	MCF-7	breast:
36	chr4:7084172..7086960-chr4:7087354..7090208,2	K562	blood:
37	chr4:7105423..7108283-chr4:7118442..7120103,2	MCF-7	breast:
38	chr4:6783899..6786313-chr4:7103315..7105730,2	K562	blood:
39	chr4:7084172..7086960-chr4:7087354..7090208,2	K562	blood:
40	chr4:7115313..7118277-chr4:7121147..7123527,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRPEL1-1	chr4:7096326-7096470	NONHSAT095046
2	lnc-GRPEL1-1	chr4:7099050-7099106	ENSG00000245562
3	lnc-GRPEL1-1	chr4:7104995-7105139	NONHSAT095046
4	lnc-GRPEL1-1	chr4:7099080-7099106	XLOC_003872
5	lnc-GRPEL1-1	chr4:7096298-7096470	ENSG00000245562
6	lnc-GRPEL1-1	chr4:7099151-7101181	XLOC_003872
7	lnc-GRPEL1-1	chr4:7099050-7099106	NONHSAT095046
8	lnc-GRPEL1-1	chr4:7102967-7105112	ENSG00000245468
9	lnc-GRPEL1-1	chr4:7104995-7105186	XLOC_003872
10	lnc-GRPEL1-1	chr4:7099795-7101181	ENSG00000245562
11	lnc-GRPEL1-1	chr4:7104995-7105107	ENSG00000245562
12	lnc-GRPEL1-1	chr4:7104995-7105103	XLOC_003872
13	lnc-GRPEL1-1	chr4:7104995-7105056	ENSG00000245562

No data

Variant related genes	Relation type
ENSG00000245468	TF binding region
RN7SKP36	TF binding region
ENSG00000245468	CpG island
RN7SKP36	CpG island
ENSG00000109519	chromatin interactions
ENSG00000200867	chromatin interactions
ENSG00000170871	chromatin interactions
ENSG00000245468	chromatin interactions
ENSG00000173011	chromatin interactions
ENSG00000173013	chromatin interactions
KIAA1274	miRNA target sites
TUSC2	miRNA target sites
RBM19	miRNA target sites
ERAP2	miRNA target sites
RIOK3	miRNA target sites

Extended variants
information (count: 1609 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1609 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3857184	chr4:7084985-7084986	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574277643	chr4:7084989-7084990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74989892	chr4:7084990-7084991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77756866	chr4:7084991-7084992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs3857185	chr4:7085004-7085005	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs577376453	chr4:7085034-7085035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112403387	chr4:7085055-7085056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538458405	chr4:7085085-7085086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563598037	chr4:7085136-7085137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116211274	chr4:7085153-7085154	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572289295	chr4:7085198-7085199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542987464	chr4:7085221-7085222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182885593	chr4:7085326-7085327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576520603	chr4:7085376-7085377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187956074	chr4:7085394-7085395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576400711	chr4:7085402-7085403	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375066635	chr4:7085453-7085454	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143067808	chr4:7085509-7085510	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532738649	chr4:7085519-7085520	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552831279	chr4:7085525-7085526	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190922587	chr4:7085530-7085531	Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs367557957	chr4:7085610-7085611	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs541294489	chr4:7085622-7085623	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3857186	chr4:7085632-7085633	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4026587	chr4:7085637-7085638	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373558533	chr4:7085640-7085641	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367690885	chr4:7085652-7085653	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs3857187	chr4:7085662-7085663	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4082842	chr4:7085664-7085665	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559979671	chr4:7085669-7085670	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs548028543	chr4:7085683-7085684	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530352663	chr4:7085738-7085739	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548491897	chr4:7085758-7085759	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566885853	chr4:7085766-7085767	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76121146	chr4:7085786-7085787	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1877411	chr4:7085794-7085795	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183972662	chr4:7085868-7085869	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs138617501	chr4:7085882-7085883	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs187718111	chr4:7085883-7085884	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs553713929	chr4:7085916-7085917	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
41	rs141494990	chr4:7085930-7085931	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
42	rs536517275	chr4:7085974-7085975	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
43	rs371250288	chr4:7085982-7085983	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs554912347	chr4:7085998-7085999	Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs530311498	chr4:7086009-7086010	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs55812547	chr4:7086054-7086055	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs543887690	chr4:7086123-7086124	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114369939	chr4:7086184-7086185	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570286721	chr4:7086241-7086242	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs541589105	chr4:7086251-7086252	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:766 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7071000-7086200	Weak transcription	Right Atrium	heart
2	chr4:7078200-7086000	Weak transcription	Pancreas	Pancrea
3	chr4:7078800-7085000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:7083000-7085000	Enhancers	K562	blood
5	chr4:7084200-7085800	Weak transcription	Liver	Liver
6	chr4:7084200-7085800	Weak transcription	Ovary	ovary
7	chr4:7084600-7085000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:7085000-7085200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:7085000-7085800	Weak transcription	K562	blood
10	chr4:7085200-7085600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:7085400-7086200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
12	chr4:7085600-7086200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:7085800-7086000	Enhancers	Liver	Liver
14	chr4:7085800-7086000	Bivalent/Poised TSS	Hela-S3	cervix
15	chr4:7085800-7086000	Flanking Bivalent TSS/Enh	HepG2	liver
16	chr4:7085800-7086200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
17	chr4:7085800-7086200	Active TSS	Skeletal Muscle Female	skeletal muscle
18	chr4:7085800-7086200	Enhancers	K562	blood
19	chr4:7085800-7086400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
20	chr4:7085800-7086400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
21	chr4:7085800-7086600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
22	chr4:7085800-7086600	Active TSS	A549	lung
23	chr4:7085800-7087000	Enhancers	Ovary	ovary
24	chr4:7086000-7086200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr4:7086000-7086200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:7086000-7086200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
27	chr4:7086000-7086200	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
28	chr4:7086000-7086400	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:7086000-7086400	Bivalent/Poised TSS	Adipose Nuclei	Adipose
30	chr4:7086000-7086400	Flanking Active TSS	Liver	Liver
31	chr4:7086000-7086400	Bivalent/Poised TSS	Colonic Mucosa	Colon
32	chr4:7086000-7086400	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr4:7086000-7086400	Enhancers	Pancreas	Pancrea
34	chr4:7086000-7086400	Active TSS	Hela-S3	cervix
35	chr4:7086000-7086400	Bivalent/Poised TSS	NHEK	skin
36	chr4:7086000-7086600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:7086000-7086800	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr4:7086000-7086800	Active TSS	HepG2	liver
39	chr4:7086200-7086400	Active TSS	Right Atrium	heart
40	chr4:7086200-7086800	Active TSS	Duodenum Mucosa	Duodenum
41	chr4:7086200-7086800	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr4:7086200-7086800	Enhancers	Stomach Mucosa	stomach
43	chr4:7086200-7087000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
44	chr4:7086200-7087000	Active TSS	K562	blood
45	chr4:7086400-7087200	Enhancers	Liver	Liver
46	chr4:7086400-7090800	Weak transcription	Pancreas	Pancrea
47	chr4:7086800-7087000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr4:7086800-7090600	Weak transcription	Stomach Mucosa	stomach
49	chr4:7087000-7090800	Weak transcription	Ovary	ovary
50	chr4:7087200-7090400	Weak transcription	Liver	Liver

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