Variant report

Variant	nsv1032630
Chromosome Location	chr4:188292185-188514608
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:603)
CpG islands
(count:671)
Chromatin interactive
region (count:12)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
2	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
3	CBX3	chr4:188301159-188301792	HCT-116	colon:	n/a	n/a
4	CBX3	chr4:188507537-188508612	HCT-116	colon:	n/a	n/a
5	CEBPB	chr4:188301254-188301599	MCF-7	breast:	n/a	n/a
6	CEBPB	chr4:188405764-188405895	H1-hESC	embryonic stem cell:	n/a	chr4:188405878-188405889 chr4:188405877-188405890
7	CEBPB	chr4:188479534-188479869	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:188301254-188301597	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:188317704-188317987	IMR90	lung:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
10	CEBPB	chr4:188440289-188440620	HepG2	liver:	n/a	n/a
11	CEBPB	chr4:188440459-188440698	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:188349162-188349196	H1-hESC	embryonic stem cell:	n/a	chr4:188349183-188349194
13	CEBPB	chr4:188337419-188337771	IMR90	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
14	CEBPB	chr4:188337469-188337769	A549	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
15	CEBPB	chr4:188492567-188492769	HepG2	liver:	n/a	chr4:188492666-188492677
16	CEBPB	chr4:188295952-188296114	HepG2	liver:	n/a	chr4:188296003-188296014 chr4:188296003-188296016
17	CEBPB	chr4:188504954-188505154	HepG2	liver:	n/a	chr4:188504994-188505011
18	CEBPB	chr4:188317722-188317931	HepG2	liver:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
19	CEBPB	chr4:188406167-188406450	A549	lung:	n/a	n/a
20	CEBPB	chr4:188309832-188310058	IMR90	lung:	n/a	chr4:188309977-188309986
21	CEBPB	chr4:188301323-188301523	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr4:188401324-188401855	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:188376676-188376735	HepG2	liver:	n/a	chr4:188376676-188376689 chr4:188376676-188376687 chr4:188376678-188376689
24	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
25	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
26	CEBPB	chr4:188509334-188509409	HepG2	liver:	n/a	chr4:188509373-188509384
27	CEBPB	chr4:188301252-188301594	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:188474103-188474183	K562	blood:	n/a	n/a
29	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
30	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
32	CEBPB	chr4:188492564-188492757	K562	blood:	n/a	chr4:188492666-188492677
33	CEBPB	chr4:188405581-188406417	HepG2	liver:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
34	CEBPB	chr4:188337488-188337650	K562	blood:	n/a	chr4:188337610-188337621
35	CTCF	chr4:188338000-188338150	HCT-116	colon:	n/a	n/a
36	CTCF	chr4:188301300-188301450	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr4:188301340-188301490	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr4:188301332-188301500	LNCaP	prostate:	n/a	n/a
39	CTCF	chr4:188301282-188301522	Gliobla	brain:	n/a	n/a
40	CTCF	chr4:188301301-188301509	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:188301320-188301470	AG04449	skin:	n/a	n/a
42	CTCF	chr4:188301200-188301350	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr4:188301340-188301490	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr4:188301320-188301470	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr4:188337997-188338068	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:188301320-188301470	NHEK	skin:	n/a	n/a
47	CTCF	chr4:188301300-188301450	HPF	lung:	n/a	n/a
48	CTCF	chr4:188301300-188301450	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr4:188337968-188338082	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:188301300-188301450	AG09309	skin:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188401038-188401088	PANC-1	pancreas:	n/a
2	chr4:188462685-188462735	SKMC	muscle:	n/a
3	chr4:188426437-188426487	NH-A	brain:	n/a
4	chr4:188426278-188426328	HMEC	breast:	n/a
5	chr4:188427966-188428016	SK-N-SH_RA	brain:	n/a
6	chr4:188426506-188426556	GM19239	blood:	n/a
7	chr4:188462685-188462735	SK-N-SH	brain:	n/a
8	chr4:188314314-188314364	Caco-2	colon:	n/a
9	chr4:188401038-188401088	Hepatocyte	liver:	n/a
10	chr4:188426506-188426556	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:188427966-188428016	PrEC	prostate:	n/a
12	chr4:188426437-188426487	HCT-116	colon:	n/a
13	chr4:188427966-188428016	NHDF-neo	bronchial:	n/a
14	chr4:188427966-188428016	H1-hESC	embryonic stem cell:	embryo
15	chr4:188426506-188426556	ovcar-3	ovarian:	n/a
16	chr4:188423066-188423116	HNPCEpiC	eye:	n/a
17	chr4:188314314-188314364	AG04449	skin:	fetal
18	chr4:188426506-188426556	NHBE	bronchial:	n/a
19	chr4:188428637-188428687	HL-60	blood:	n/a
20	chr4:188401038-188401088	AoSMC	blood vessel:	n/a
21	chr4:188314314-188314364	HIPEpiC	eye:	n/a
22	chr4:188426278-188426328	HEEpiC	esophagus:	n/a
23	chr4:188428637-188428687	H1-hESC	embryonic stem cell:	embryo
24	chr4:188423066-188423116	HEEpiC	esophagus:	n/a
25	chr4:188398437-188398487	ovcar-3	ovarian:	n/a
26	chr4:188398437-188398487	H1-hESC	embryonic stem cell:	embryo
27	chr4:188423066-188423116	HRCEpiC	kidney:	n/a
28	chr4:188427966-188428016	AG09319	gingival:	n/a
29	chr4:188314314-188314364	HNPCEpiC	eye:	n/a
30	chr4:188428637-188428687	SK-N-SH	brain:	n/a
31	chr4:188426278-188426328	AG04450	lung:	fetal
32	chr4:188426506-188426556	HRCEpiC	kidney:	n/a
33	chr4:188401038-188401088	HCT-116	colon:	n/a
34	chr4:188426278-188426328	NHDF-neo	bronchial:	n/a
35	chr4:188314314-188314364	HCT-116	colon:	n/a
36	chr4:188314314-188314364	BJ	skin:	n/a
37	chr4:188391387-188391437	HUVEC	blood vessel:	n/a
38	chr4:188398437-188398487	PANC-1	pancreas:	n/a
39	chr4:188426437-188426487	HNPCEpiC	eye:	n/a
40	chr4:188428637-188428687	HNPCEpiC	eye:	n/a
41	chr4:188428637-188428687	MCF10A-Er-Src	breast:	n/a
42	chr4:188427966-188428016	BE2_C	brain:	n/a
43	chr4:188314314-188314364	ProgFib	skin:	n/a
44	chr4:188398437-188398487	HRE	kidney:	n/a
45	chr4:188426437-188426487	U87	brain:	n/a
46	chr4:188426506-188426556	HL-60	blood:	n/a
47	chr4:188398437-188398487	SKMC	muscle:	n/a
48	chr4:188401038-188401088	Jurkat	blood:	n/a
49	chr4:188398437-188398487	GM19239	blood:	n/a
50	chr4:188427966-188428016	HPAEpiC	pulmonary alveolar:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
2	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
3	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
4	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
5	chr4:188426813..188429681-chrX:150150480..150152156,2	MCF-7	breast:
6	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
7	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
8	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
9	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
10	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
11	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
12	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
2	lnc-ZFP42-4	chr4:188351216-188351539	XLOC_003828
3	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
4	lnc-TRIML2-4	chr4:188503575-188503684	ENSG00000250590
5	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
6	lnc-ZFP42-4	chr4:188344049-188344151	XLOC_003828
7	lnc-ZFP42-10	chr4:188493477-188493987	NONHSAT099705
8	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
9	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590
10	lnc-TRIML2-5	chr4:188438236-188438362	XLOC_004219
11	lnc-TRIML2-4	chr4:188513897-188514081	NONHSAT099704
12	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704
13	lnc-ZFP42-6	chr4:188292838-188293075	XLOC_003826
14	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
15	lnc-TRIML2-4	chr4:188478901-188479074	ENSG00000250590
16	lnc-ZFP42-5	chr4:188336464-188337128	NONHSAT099694
17	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
18	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
19	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
20	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
21	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
22	lnc-TRIML2-4	chr4:188454033-188454357	NR_110436
23	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590
24	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
25	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
26	lnc-TRIML2-4	chr4:188514038-188514081	ENSG00000250590
27	lnc-TRIML2-4	chr4:188454036-188454357	ENSG00000250590
28	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
29	lnc-ZFP42-10	chr4:188501769-188501890	NONHSAT099705
30	lnc-TRIML2-4	chr4:188513797-188514081	NONHSAT099706
31	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620
32	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
33	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
34	lnc-ZFP42-6	chr4:188292449-188292580	XLOC_003826
35	lnc-ZFP42-5	chr4:188334716-188334865	NONHSAT099694
36	lnc-TRIML2-5	chr4:188437307-188437878	XLOC_004219
37	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
38	lnc-ZFP42-5	chr4:188334718-188334865	ENSG00000250620

No data

Variant related genes	Relation type
ENSG00000251490	TF binding region
ENSG00000251643	TF binding region
ENSG00000250620	TF binding region
ENSG00000250590	TF binding region
ENSG00000251490	CpG island
ENSG00000251643	CpG island
ENSG00000250620	CpG island
ENSG00000250590	CpG island
ENSG00000251643	chromatin interactions
ENSG00000029993	chromatin interactions
ANP32E	miRNA target sites
ANTXR1	miRNA target sites

Extended variants
information (count: 4609 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4609 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541235325	chr4:188292207-188292208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs11942521	chr4:188292264-188292265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532697250	chr4:188292292-188292293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373852584	chr4:188292300-188292301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562709400	chr4:188292356-188292357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531756747	chr4:188292380-188292381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576785451	chr4:188292406-188292407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544504327	chr4:188292435-188292436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563034508	chr4:188292517-188292518	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs530355773	chr4:188292530-188292531	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs568746728	chr4:188292574-188292575	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs564348477	chr4:188292580-188292581	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs528723425	chr4:188292633-188292634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547632999	chr4:188292667-188292668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570191997	chr4:188292682-188292683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539181745	chr4:188292700-188292701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186795611	chr4:188292769-188292770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575919405	chr4:188292775-188292776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554401032	chr4:188292804-188292805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546908753	chr4:188292834-188292835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148931907	chr4:188292841-188292842	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs572773838	chr4:188292870-188292871	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs555331311	chr4:188292960-188292961	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs572408818	chr4:188292968-188292969	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs541222860	chr4:188292988-188292989	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs564298849	chr4:188292989-188292990	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs577399052	chr4:188293011-188293012	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs143679337	chr4:188293052-188293053	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs563005344	chr4:188293080-188293081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72723263	chr4:188293088-188293089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191637541	chr4:188293092-188293093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562242034	chr4:188293101-188293102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148059876	chr4:188293170-188293171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183967669	chr4:188293180-188293181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570676683	chr4:188293206-188293207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188912146	chr4:188293238-188293239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191910572	chr4:188293268-188293269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182283047	chr4:188293288-188293289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535093709	chr4:188293289-188293290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186635391	chr4:188293329-188293330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375872854	chr4:188293389-188293390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56391790	chr4:188293401-188293402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs191837944	chr4:188293416-188293417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534948372	chr4:188293442-188293443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9992540	chr4:188293457-188293458	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs577867956	chr4:188293471-188293472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569699339	chr4:188293477-188293478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183819306	chr4:188293497-188293498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188476650	chr4:188293506-188293507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs193045448	chr4:188293539-188293540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188291800-188292600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:188291800-188292800	Enhancers	Fetal Heart	heart
3	chr4:188292000-188292200	Enhancers	Fetal Intestine Large	intestine
4	chr4:188292600-188294800	Weak transcription	Fetal Intestine Large	intestine
5	chr4:188292600-188304000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:188294600-188295200	Enhancers	Adipose Nuclei	Adipose
7	chr4:188294800-188295000	Enhancers	Fetal Intestine Large	intestine
8	chr4:188294800-188295000	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr4:188295000-188295600	Weak transcription	Fetal Intestine Large	intestine
10	chr4:188295200-188299200	Weak transcription	Adipose Nuclei	Adipose
11	chr4:188295600-188295800	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr4:188295600-188296600	Enhancers	Fetal Intestine Large	intestine
13	chr4:188297800-188298400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:188299200-188300000	Enhancers	Adipose Nuclei	Adipose
15	chr4:188301400-188301800	Enhancers	Pancreas	Pancrea
16	chr4:188301800-188304000	Weak transcription	Pancreas	Pancrea
17	chr4:188304000-188304600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:188304000-188304600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:188304200-188304800	Enhancers	HMEC	breast
20	chr4:188308400-188308600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr4:188308400-188309000	Enhancers	A549	lung
22	chr4:188308600-188309200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr4:188309000-188309400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:188309000-188309400	Flanking Active TSS	A549	lung
25	chr4:188309000-188309800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr4:188309200-188310000	Enhancers	Placenta Amnion	Placenta Amnion
27	chr4:188309400-188309600	Enhancers	A549	lung
28	chr4:188309800-188311000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:188310000-188310400	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr4:188310400-188310800	Enhancers	Placenta Amnion	Placenta Amnion
31	chr4:188311000-188311200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:188314200-188316000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:188314400-188315600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr4:188314800-188315000	Enhancers	NHLF	lung
35	chr4:188314800-188315600	Enhancers	NHDF-Ad	bronchial
36	chr4:188319600-188319800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:188321400-188322000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:188323200-188338800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:188329000-188329600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr4:188329400-188330000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:188335600-188337800	Enhancers	Fetal Brain Male	brain
42	chr4:188335800-188336000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:188335800-188336200	Enhancers	Fetal Muscle Leg	muscle
44	chr4:188335800-188339400	Enhancers	Fetal Lung	lung
45	chr4:188336000-188336800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr4:188336000-188337800	Enhancers	Fetal Heart	heart
47	chr4:188336200-188336800	Enhancers	Adipose Nuclei	Adipose
48	chr4:188336200-188336800	Enhancers	HSMM	muscle
49	chr4:188336800-188338800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr4:188336800-188339000	Weak transcription	Adipose Nuclei	Adipose

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