Variant report

Variant	nsv537476
Chromosome Location	chr4:189137071-189407890
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1525)
CpG islands
(count:2383)
Chromatin interactive
region (count:8)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:189324598-189324718	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:189376606-189376828	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:189359441-189359980	HepG2	liver:	n/a	n/a
4	ATF2	chr4:189320870-189321336	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:189320962-189321575	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:189324595-189324738	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:189366501-189366863	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:189353505-189353712	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:189321022-189321611	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:189370074-189371014	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:189203531-189203904	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:189308557-189308573	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:189365427-189366156	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:189372985-189373571	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr4:189312088-189312284	GM12878	blood:	n/a	chr4:189312224-189312235
16	BCL11A	chr4:189373274-189373489	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr4:189320997-189321292	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr4:189344161-189344742	A549	lung:	n/a	n/a
19	BCL3	chr4:189247008-189247247	GM12878	blood:	n/a	n/a
20	BCL3	chr4:189370110-189370622	A549	lung:	n/a	n/a
21	BCL3	chr4:189246967-189247207	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:189324559-189324730	HepG2	liver:	n/a	n/a
23	BHLHE40	chr4:189167743-189167747	K562	blood:	n/a	n/a
24	BHLHE40	chr4:189291962-189292207	GM12878	blood:	n/a	n/a
25	BRCA1	chr4:189404735-189404847	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr4:189324508-189324656	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr4:189304915-189305326	HCT-116	colon:	n/a	n/a
28	CEBPB	chr4:189262860-189263130	K562	blood:	n/a	chr4:189263022-189263033
29	CEBPB	chr4:189216845-189217381	IMR90	lung:	n/a	chr4:189216947-189216964 chr4:189217187-189217198 chr4:189217185-189217198 chr4:189217187-189217198 chr4:189217185-189217198 chr4:189216949-189216960 chr4:189217185-189217198
30	CEBPB	chr4:189321942-189322198	HepG2	liver:	n/a	chr4:189322034-189322045
31	CEBPB	chr4:189288202-189288489	IMR90	lung:	n/a	chr4:189288365-189288376
32	CEBPB	chr4:189380428-189380719	HepG2	liver:	n/a	chr4:189380547-189380558
33	CEBPB	chr4:189196510-189196762	HepG2	liver:	n/a	chr4:189196648-189196659
34	CEBPB	chr4:189288199-189288526	HepG2	liver:	n/a	chr4:189288365-189288376
35	CEBPB	chr4:189262870-189263143	A549	lung:	n/a	chr4:189263022-189263033
36	CEBPB	chr4:189216908-189217275	A549	lung:	n/a	chr4:189216947-189216964 chr4:189217187-189217198 chr4:189217185-189217198 chr4:189217187-189217198 chr4:189217185-189217198 chr4:189216949-189216960 chr4:189217185-189217198
37	CEBPB	chr4:189365679-189366052	IMR90	lung:	n/a	chr4:189365858-189365869
38	CEBPB	chr4:189365695-189366033	Hela-S3	cervix:	n/a	chr4:189365858-189365869
39	CEBPB	chr4:189203810-189204281	H1-hESC	embryonic stem cell:	n/a	chr4:189204116-189204129
40	CEBPB	chr4:189325954-189326957	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:189365674-189365990	A549	lung:	n/a	chr4:189365858-189365869
42	CEBPB	chr4:189178682-189178864	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:189262859-189263200	HepG2	liver:	n/a	chr4:189263022-189263033
44	CEBPB	chr4:189365683-189366034	A549	lung:	n/a	chr4:189365858-189365869
45	CEBPB	chr4:189250133-189250458	HepG2	liver:	n/a	n/a
46	CEBPB	chr4:189347694-189347925	A549	lung:	n/a	n/a
47	CEBPB	chr4:189351132-189351486	IMR90	lung:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
48	CEBPB	chr4:189348245-189348520	HepG2	liver:	n/a	chr4:189348399-189348410 chr4:189348381-189348392
49	CEBPB	chr4:189220329-189220641	IMR90	lung:	n/a	n/a
50	CEBPB	chr4:189183611-189184091	Hela-S3	cervix:	n/a	n/a

(count:2383 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:189376704-189376754	SAEC	small airway:	n/a
2	chr4:189158066-189158116	HCT-116	colon:	n/a
3	chr4:189333138-189333188	NH-A	brain:	n/a
4	chr4:189203962-189204012	Caco-2	colon:	n/a
5	chr4:189376704-189376754	SAEC	small airway:	n/a
6	chr4:189158066-189158116	HCT-116	colon:	n/a
7	chr4:189333138-189333188	NH-A	brain:	n/a
8	chr4:189203962-189204012	Caco-2	colon:	n/a
9	chr4:189189431-189189481	PANC-1	pancreas:	n/a
10	chr4:189376704-189376754	SK-N-SH	brain:	n/a
11	chr4:189321136-189321186	NH-A	brain:	n/a
12	chr4:189158087-189158137	MCF-7	breast:	n/a
13	chr4:189395410-189395460	NH-A	brain:	n/a
14	chr4:189191506-189191556	IMR90	lung:	fetal
15	chr4:189204296-189204346	AoSMC	blood vessel:	n/a
16	chr4:189375995-189376045	AG09309	skin:	n/a
17	chr4:189139691-189139741	AG04450	lung:	fetal
18	chr4:189376729-189376779	A549	lung:	n/a
19	chr4:189203965-189204015	Hepatocyte	liver:	n/a
20	chr4:189258348-189258398	Hepatocyte	liver:	n/a
21	chr4:189395410-189395460	PANC-1	pancreas:	n/a
22	chr4:189158022-189158072	PrEC	prostate:	n/a
23	chr4:189204589-189204639	PrEC	prostate:	n/a
24	chr4:189321136-189321186	LNCaP	prostate:	n/a
25	chr4:189200528-189200578	BJ	skin:	n/a
26	chr4:189358149-189358199	ProgFib	skin:	n/a
27	chr4:189203391-189203441	HIPEpiC	eye:	n/a
28	chr4:189203962-189204012	Hela-S3	cervix:	n/a
29	chr4:189359992-189360042	GM12891	blood:	n/a
30	chr4:189350268-189350318	AG04449	skin:	fetal
31	chr4:189158066-189158116	AG04449	skin:	fetal
32	chr4:189333449-189333499	AoSMC	blood vessel:	n/a
33	chr4:189200528-189200578	NH-A	brain:	n/a
34	chr4:189204296-189204346	HNPCEpiC	eye:	n/a
35	chr4:189203962-189204012	GM12892	blood:	n/a
36	chr4:189220624-189220674	SK-N-MC	brain:	n/a
37	chr4:189204589-189204639	AG09309	skin:	n/a
38	chr4:189258068-189258118	AG10803	skin:	n/a
39	chr4:189395410-189395460	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:189321136-189321186	HRPEpiC	eye:	n/a
41	chr4:189376704-189376754	AG10803	skin:	n/a
42	chr4:189350268-189350318	SK-N-SH_RA	brain:	n/a
43	chr4:189158087-189158137	AoSMC	blood vessel:	n/a
44	chr4:189376729-189376779	HPAEpiC	pulmonary alveolar:	n/a
45	chr4:189333296-189333346	SAEC	small airway:	n/a
46	chr4:189258195-189258245	ovcar-3	ovarian:	n/a
47	chr4:189375874-189375924	PFSK-1	brain:	n/a
48	chr4:189333449-189333499	PANC-1	pancreas:	n/a
49	chr4:189158087-189158137	T-47D	breast:	n/a
50	chr4:189330030-189330080	HPAEpiC	pulmonary alveolar:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188587219..188588049-chr4:189293834..189294448,2	MCF-7	breast:
2	chr4:188914709..188915626-chr4:189293756..189294718,5	MCF-7	breast:
3	chr4:188914670..188915671-chr4:189167438..189168869,4	MCF-7	breast:
4	chr20:30047555..30048272-chr4:189297803..189298552,2	MCF-7	breast:
5	chr4:188914697..188915636-chr4:189293778..189294511,3	MCF-7	breast:
6	chr4:188527128..188528286-chr4:189293970..189294660,4	MCF-7	breast:
7	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
8	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099745
2	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
3	lnc-TRIML1-3	chr4:189357858-189358054	ENSG00000249378
4	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
5	lnc-TRIML1-3	chr4:189377846-189377916	XLOC_003834
6	lnc-TRIML1-3	chr4:189332748-189333925	XLOC_003834
7	lnc-TRIML1-3	chr4:189321890-189321987	ENSG00000249378
8	lnc-TRIML1-3	chr4:189398792-189399066	XLOC_003834
9	lnc-TRIML1-3	chr4:189398906-189399066	NONHSAT099749
10	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
11	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099745
12	lnc-TRIML1-3	chr4:189357858-189358015	XLOC_003834
13	lnc-TRIML1-3	chr4:189376732-189376828	NONHSAT099745
14	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
15	lnc-TRIML1-3	chr4:189376732-189376828	XLOC_003834
16	lnc-TRIML1-3	chr4:189406933-189407076	NONHSAT099746
17	lnc-TRIML1-3	chr4:189357858-189358054	ENSG00000249378
18	lnc-TRIML1-3	chr4:189376747-189376828	ENSG00000249378
19	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
20	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
21	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
22	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
23	lnc-TRIML1-3	chr4:189376768-189376828	XLOC_003834
24	lnc-TRIML1-3	chr4:189376733-189376830	NONHSAT099746
25	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099746
26	lnc-TRIML1-3	chr4:189406933-189407011	XLOC_003834
27	lnc-TRIML1-3	chr4:189376735-189376828	XLOC_003834
28	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
29	lnc-TRIML2-8	chr4:189219369-189219538	NONHSAT099739
30	lnc-TRIML2-8	chr4:189222763-189222834	NONHSAT099739
31	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
32	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099749
33	lnc-TRIML1-3	chr4:189377818-189377916	ENSG00000249378
34	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099745
35	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
36	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
37	lnc-TRIML1-3	chr4:189398792-189399066	ENSG00000249378
38	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
39	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
40	lnc-TRIML1-3	chr4:189398792-189399066	NONHSAT099746
41	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099746
42	lnc-TRIML1-3	chr4:189406933-189407028	XLOC_003834
43	lnc-TRIML1-3	chr4:189321890-189321987	ENSG00000249378

No data

Variant related genes	Relation type
LINC01060	TF binding region
ENSG00000242169	TF binding region
NARG2P1	TF binding region
LINC01060	CpG island
ENSG00000242169	CpG island
NARG2P1	CpG island
C1orf144	miRNA target sites
PFN2	miRNA target sites
KCNK1	miRNA target sites
BMPR2	miRNA target sites
NCOA3	miRNA target sites
DCAF7	miRNA target sites
PRNP	miRNA target sites
SHCBP1	miRNA target sites
CREBL2	miRNA target sites
PDZD11	miRNA target sites
FAM104A	miRNA target sites
ARRDC3	miRNA target sites
RASSF2	miRNA target sites

Extended variants
information (count: 9755 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:9755 , 50 per page) page: 1 2 3 4 5 6 7 ... 196

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534160457	chr4:189137092-189137093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs199672793	chr4:189137181-189137182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11942263	chr4:189137192-189137193	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs571208163	chr4:189137214-189137215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374402170	chr4:189137223-189137224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368768773	chr4:189137226-189137227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540140313	chr4:189137238-189137239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72658802	chr4:189137248-189137249	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369008868	chr4:189137258-189137259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556555181	chr4:189137259-189137260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75382839	chr4:189137265-189137266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs36193941	chr4:189137269-189137270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs13121322	chr4:189137272-189137273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200730704	chr4:189137275-189137276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183110749	chr4:189137278-189137279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375308933	chr4:189137290-189137291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201872369	chr4:189137293-189137294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143721997	chr4:189137296-189137297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs13121512	chr4:189137320-189137321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143907506	chr4:189137329-189137330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369980711	chr4:189137331-189137332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200288538	chr4:189137341-189137342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13148810	chr4:189137349-189137350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372884647	chr4:189137350-189137351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373163069	chr4:189137352-189137353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs13121535	chr4:189137357-189137358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190450691	chr4:189137367-189137368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139164283	chr4:189137388-189137389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367570904	chr4:189137399-189137400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377135009	chr4:189137400-189137401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372873838	chr4:189137416-189137417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371643394	chr4:189137427-189137428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368705917	chr4:189137464-189137465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs376711893	chr4:189137468-189137469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187370049	chr4:189137495-189137496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369749413	chr4:189137515-189137516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560936022	chr4:189137525-189137526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368811349	chr4:189137534-189137535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151173912	chr4:189137542-189137543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373501349	chr4:189137545-189137546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376869504	chr4:189137569-189137570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111205910	chr4:189137580-189137581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368716233	chr4:189137582-189137583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111205911	chr4:189137583-189137584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373128117	chr4:189137593-189137594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376280465	chr4:189137594-189137595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201011610	chr4:189137614-189137615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201646429	chr4:189137626-189137627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183705585	chr4:189137642-189137643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370829489	chr4:189137651-189137652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Cognitive impairment	21505072	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	20808228	CNVD
Epilepsy	21635232	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1083 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:189130200-189139400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:189137800-189138200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:189137800-189140000	Enhancers	Fetal Brain Male	brain
4	chr4:189139000-189139200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:189139000-189139200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr4:189139200-189139400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:189139200-189139400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr4:189139200-189139400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:189139200-189139600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr4:189139200-189139800	Active TSS	H9 Cell Line	embryonic stem cell
11	chr4:189139200-189139800	Active TSS	iPS-20b Cell Line	embryonic stem cell
12	chr4:189139200-189140200	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr4:189139200-189140200	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr4:189139400-189139600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:189139400-189139800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:189139400-189139800	Active TSS	HUES64 Cell Line	embryonic stem cell
17	chr4:189139400-189139800	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr4:189139400-189139800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:189139400-189139800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:189139400-189140000	Active TSS	H1 Cell Line	embryonic stem cell
21	chr4:189139400-189140000	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr4:189139400-189140000	Enhancers	Fetal Stomach	stomach
23	chr4:189139600-189139800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr4:189139600-189139800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
25	chr4:189139600-189140000	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr4:189139600-189140200	Bivalent Enhancer	Placenta	Placenta
27	chr4:189139800-189140000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:189139800-189140000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:189139800-189140000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr4:189140000-189140200	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:189140000-189141000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:189140200-189140400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr4:189140200-189141000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:189140200-189144200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr4:189140400-189141200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr4:189140800-189141600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:189144400-189144800	Enhancers	Fetal Heart	heart
38	chr4:189147000-189147400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr4:189152000-189152200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:189152600-189153000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr4:189152600-189153000	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr4:189152800-189153000	ZNF genes & repeats	Fetal Kidney	kidney
43	chr4:189153000-189157400	Weak transcription	Fetal Kidney	kidney
44	chr4:189157600-189157800	Enhancers	Fetal Kidney	kidney
45	chr4:189166200-189167000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:189166400-189166800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:189168200-189169600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:189173600-189174000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:189174000-189175400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr4:189175400-189175600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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