Variant report

Variant	nsv537486
Chromosome Location	chr4:189258025-189510368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1424)
CpG islands
(count:1406)
Chromatin interactive
region (count:8)
LncRNA
region (count:42)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:189456095-189456482	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:189455499-189455789	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:189359441-189359980	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:189324598-189324718	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:189499935-189500273	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:189376606-189376828	HepG2	liver:	n/a	n/a
7	ATF2	chr4:189320962-189321575	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:189320870-189321336	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	chr4:189353505-189353712	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	chr4:189324595-189324738	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:189365427-189366156	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:189372985-189373571	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr4:189366501-189366863	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr4:189312088-189312284	GM12878	blood:	n/a	chr4:189312224-189312235
18	BCL11A	chr4:189373274-189373489	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr4:189320997-189321292	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL3	chr4:189344161-189344742	A549	lung:	n/a	n/a
21	BCL3	chr4:189370110-189370622	A549	lung:	n/a	n/a
22	BHLHE40	chr4:189456176-189456442	HepG2	liver:	n/a	n/a
23	BHLHE40	chr4:189291962-189292207	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:189324559-189324730	HepG2	liver:	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	chr4:189351041-189351582	A549	lung:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
29	CEBPB	chr4:189324423-189324584	A549	lung:	n/a	n/a
30	CEBPB	chr4:189347694-189347925	A549	lung:	n/a	n/a
31	CEBPB	chr4:189348245-189348520	HepG2	liver:	n/a	chr4:189348399-189348410 chr4:189348381-189348392
32	CEBPB	chr4:189365695-189366033	Hela-S3	cervix:	n/a	chr4:189365858-189365869
33	CEBPB	chr4:189321942-189322198	HepG2	liver:	n/a	chr4:189322034-189322045
34	CEBPB	chr4:189365565-189366090	A549	lung:	n/a	chr4:189365858-189365869
35	CEBPB	chr4:189456046-189456370	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:189370569-189370830	A549	lung:	n/a	n/a
37	CEBPB	chr4:189262870-189263143	A549	lung:	n/a	chr4:189263022-189263033
38	CEBPB	chr4:189262873-189263190	IMR90	lung:	n/a	chr4:189263022-189263033
39	CEBPB	chr4:189493631-189493895	A549	lung:	n/a	chr4:189493776-189493787
40	CEBPB	chr4:189351138-189351492	A549	lung:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
41	CEBPB	chr4:189262860-189263130	K562	blood:	n/a	chr4:189263022-189263033
42	CEBPB	chr4:189380428-189380719	HepG2	liver:	n/a	chr4:189380547-189380558
43	CEBPB	chr4:189351143-189351497	H1-hESC	embryonic stem cell:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
44	CEBPB	chr4:189351129-189351501	HepG2	liver:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
45	CEBPB	chr4:189351132-189351486	IMR90	lung:	n/a	chr4:189351309-189351318 chr4:189351309-189351318 chr4:189351309-189351318
46	CEBPB	chr4:189365740-189365940	H1-hESC	embryonic stem cell:	n/a	chr4:189365858-189365869
47	CEBPB	chr4:189262856-189263109	H1-hESC	embryonic stem cell:	n/a	chr4:189263022-189263033
48	CEBPB	chr4:189323007-189323333	IMR90	lung:	n/a	n/a
49	CEBPB	chr4:189424052-189424344	IMR90	lung:	n/a	chr4:189424170-189424181
50	CEBPB	chr4:189365829-189365901	K562	blood:	n/a	chr4:189365858-189365869

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:189375995-189376045	AG04450	lung:	fetal
2	chr4:189395410-189395460	HUVEC	blood vessel:	n/a
3	chr4:189258195-189258245	HRE	kidney:	n/a
4	chr4:189375995-189376045	AG04450	lung:	fetal
5	chr4:189395410-189395460	HUVEC	blood vessel:	n/a
6	chr4:189258195-189258245	HRE	kidney:	n/a
7	chr4:189330030-189330080	HRE	kidney:	n/a
8	chr4:189258348-189258398	HCF	heart:	n/a
9	chr4:189358149-189358199	HUVEC	blood vessel:	n/a
10	chr4:189258195-189258245	AG04450	lung:	fetal
11	chr4:189333138-189333188	Hela-S3	cervix:	n/a
12	chr4:189376704-189376754	SK-N-MC	brain:	n/a
13	chr4:189476613-189476663	CMK	blood:	n/a
14	chr4:189258195-189258245	HCF	heart:	n/a
15	chr4:189321136-189321186	PrEC	prostate:	n/a
16	chr4:189321244-189321294	HCT-116	colon:	n/a
17	chr4:189375874-189375924	HRPEpiC	eye:	n/a
18	chr4:189333138-189333188	HepG2	liver:	n/a
19	chr4:189359992-189360042	U87	brain:	n/a
20	chr4:189330030-189330080	SK-N-SH	brain:	n/a
21	chr4:189485260-189485310	HEEpiC	esophagus:	n/a
22	chr4:189330030-189330080	HUVEC	blood vessel:	n/a
23	chr4:189333138-189333188	LNCaP	prostate:	n/a
24	chr4:189476745-189476795	T-47D	breast:	n/a
25	chr4:189375874-189375924	T-47D	breast:	n/a
26	chr4:189330030-189330080	AG10803	skin:	n/a
27	chr4:189375874-189375924	HCT-116	colon:	n/a
28	chr4:189321244-189321294	SKMC	muscle:	n/a
29	chr4:189258348-189258398	HCPEpiC	choroid plexus:	n/a
30	chr4:189321136-189321186	AG10803	skin:	n/a
31	chr4:189321244-189321294	HAEpiC	amniotic membrane:	n/a
32	chr4:189376670-189376720	Caco-2	colon:	n/a
33	chr4:189485260-189485310	SK-N-MC	brain:	n/a
34	chr4:189376704-189376754	SKMC	muscle:	n/a
35	chr4:189359992-189360042	AG10803	skin:	n/a
36	chr4:189258195-189258245	HCM	heart:	n/a
37	chr4:189376670-189376720	HIPEpiC	eye:	n/a
38	chr4:189321244-189321294	HEEpiC	esophagus:	n/a
39	chr4:189358149-189358199	PFSK-1	brain:	n/a
40	chr4:189376704-189376754	AG04450	lung:	fetal
41	chr4:189333138-189333188	BE2_C	brain:	n/a
42	chr4:189321136-189321186	GM12878	blood:	n/a
43	chr4:189375874-189375924	HEK293	kidney:	embryo
44	chr4:189476745-189476795	AG09309	skin:	n/a
45	chr4:189321701-189321751	ovcar-3	ovarian:	n/a
46	chr4:189359992-189360042	HCPEpiC	choroid plexus:	n/a
47	chr4:189485260-189485310	Caco-2	colon:	n/a
48	chr4:189350268-189350318	SK-N-SH_RA	brain:	n/a
49	chr4:189350268-189350318	BJ	skin:	n/a
50	chr4:189376704-189376754	HAEpiC	amniotic membrane:	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	chr4:189427438..189430236-chr6:107435359..107438052,2	MCF-7	breast:
3	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
4	chr4:188914709..188915626-chr4:189293756..189294718,5	MCF-7	breast:
5	chr20:30047555..30048272-chr4:189297803..189298552,2	MCF-7	breast:
6	chr4:189390737..189392481-chr4:189394126..189396910,2	K562	blood:
7	chr4:188914697..188915636-chr4:189293778..189294511,3	MCF-7	breast:
8	chr4:188527128..188528286-chr4:189293970..189294660,4	MCF-7	breast:

(count:42 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML1-3	chr4:189398792-189399066	NONHSAT099746
2	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099745
3	lnc-TRIML1-3	chr4:189398792-189399066	XLOC_003834
4	lnc-TRIML1-3	chr4:189398906-189399066	NONHSAT099749
5	lnc-TRIML1-3	chr4:189357858-189358054	ENSG00000249378
6	lnc-TRIML1-3	chr4:189377818-189377916	ENSG00000249378
7	lnc-TRIML1-3	chr4:189357858-189358015	XLOC_003834
8	lnc-TRIML1-3	chr4:189398792-189399066	ENSG00000249378
9	lnc-TRIML1-3	chr4:189406933-189407011	XLOC_003834
10	lnc-TRIML1-3	chr4:189397852-189397910	NONHSAT099746
11	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
12	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
13	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099745
14	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099745
15	lnc-TRIML1-3	chr4:189377818-189377916	NONHSAT099746
16	lnc-TRIML1-3	chr4:189406933-189407076	NONHSAT099746
17	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
18	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
19	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
20	lnc-TRIML1-3	chr4:189376735-189376828	XLOC_003834
21	lnc-TRIML1-3	chr4:189376732-189376828	XLOC_003834
22	lnc-TRIML1-3	chr4:189376732-189376828	NONHSAT099745
23	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
24	lnc-TRIML1-3	chr4:189406933-189407028	XLOC_003834
25	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
26	lnc-TRIML1-3	chr4:189332748-189333925	XLOC_003834
27	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
28	lnc-TRIML1-3	chr4:189376747-189376828	ENSG00000249378
29	lnc-TRIML1-3	chr4:189397852-189397910	XLOC_003834
30	lnc-TRIML1-3	chr4:189457889-189459706	XLOC_003834
31	lnc-TRIML1-3	chr4:189377846-189377916	XLOC_003834
32	lnc-TRIML1-3	chr4:189377818-189377916	XLOC_003834
33	lnc-TRIML1-3	chr4:189321890-189321987	ENSG00000249378
34	lnc-TRIML1-3	chr4:189321890-189321987	ENSG00000249378
35	lnc-TRIML1-3	chr4:189376733-189376830	NONHSAT099746
36	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
37	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099749
38	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
39	lnc-TRIML1-3	chr4:189376768-189376828	XLOC_003834
40	lnc-TRIML1-3	chr4:189397852-189397910	ENSG00000249378
41	lnc-TRIML1-3	chr4:189357858-189358054	ENSG00000249378
42	lnc-TRIML1-3	chr4:189406933-189407019	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
ENSG00000178409	chromatin interactions
ARRDC3	miRNA target sites
DCAF7	miRNA target sites
BMPR2	miRNA target sites
C1orf144	miRNA target sites
PDZD11	miRNA target sites
PFN2	miRNA target sites
RASSF2	miRNA target sites
PRNP	miRNA target sites
FAM104A	miRNA target sites
CREBL2	miRNA target sites
KCNK1	miRNA target sites
NCOA3	miRNA target sites
SHCBP1	miRNA target sites

Extended variants
information (count: 10997 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:10997 , 50 per page) page: 1 2 3 4 5 6 7 ... 220

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553742690	chr4:189258189-189258190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576793437	chr4:189258196-189258197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528620732	chr4:189258200-189258201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556107925	chr4:189258207-189258208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542347825	chr4:189258222-189258223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576231252	chr4:189258224-189258225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541941805	chr4:189258225-189258226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113942998	chr4:189258229-189258230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115660482	chr4:189258255-189258256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540921231	chr4:189258259-189258260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs560598910	chr4:189258305-189258306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374473624	chr4:189258312-189258313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10008980	chr4:189258322-189258323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370752439	chr4:189258333-189258334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568683680	chr4:189258343-189258344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183062998	chr4:189258353-189258354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548267833	chr4:189258364-189258365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528395310	chr4:189258459-189258460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188150991	chr4:189258480-189258481	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs62354058	chr4:189258519-189258520	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550720391	chr4:189258552-189258553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547684341	chr4:189258554-189258555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570688685	chr4:189258559-189258560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539696237	chr4:189258585-189258586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34847136	chr4:189258595-189258596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375171224	chr4:189258636-189258637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs62354059	chr4:189258648-189258649	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs192904126	chr4:189258677-189258678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535551738	chr4:189258701-189258702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185109612	chr4:189258766-189258767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539714094	chr4:189258811-189258812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555451565	chr4:189258830-189258831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575110478	chr4:189258836-189258837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540440995	chr4:189258867-189258868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554329804	chr4:189258874-189258875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577497353	chr4:189258887-189258888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149281362	chr4:189258891-189258892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187907271	chr4:189258910-189258911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531558239	chr4:189258920-189258921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560911873	chr4:189258976-189258977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561813072	chr4:189258979-189258980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111831483	chr4:189258984-189258985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375793805	chr4:189258985-189258986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs528633011	chr4:189262012-189262013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552125811	chr4:189262029-189262030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4863029	chr4:189262049-189262050	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs531216532	chr4:189262052-189262053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs551041666	chr4:189262093-189262094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567655834	chr4:189262101-189262102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536758150	chr4:189262129-189262130	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:904 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:189257600-189258400	Enhancers	Placenta	Placenta
2	chr4:189258200-189258400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:189258200-189259000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:189262000-189262800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr4:189267400-189267800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:189270800-189271200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:189274200-189274400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
8	chr4:189274200-189282400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:189274400-189274800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr4:189278200-189278600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:189278600-189278800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr4:189278600-189279200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:189278800-189279200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr4:189279600-189279800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:189280000-189283600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:189282400-189282600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:189282400-189282600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr4:189282400-189283000	Enhancers	Placenta Amnion	Placenta Amnion
19	chr4:189282600-189283800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:189282600-189283800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr4:189283600-189284000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:189283600-189284200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:189283800-189284000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:189283800-189284200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:189283800-189284400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:189284000-189284400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:189286000-189286200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr4:189286800-189287200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:189287200-189288800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:189288200-189289000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:189288800-189289400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:189289400-189290600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:189292000-189292200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:189292000-189292200	Enhancers	A549	lung
35	chr4:189292000-189292400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:189292200-189293200	Weak transcription	A549	lung
37	chr4:189292200-189293800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:189292400-189292800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:189292800-189293400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:189292800-189294000	Enhancers	HMEC	breast
41	chr4:189292800-189294200	Enhancers	Osteobl	bone
42	chr4:189293000-189293600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:189293000-189293800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr4:189293000-189294000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:189293000-189294200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr4:189293000-189294200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:189293000-189294400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr4:189293000-189294400	Enhancers	Hela-S3	cervix
49	chr4:189293200-189293800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:189293200-189294000	Enhancers	A549	lung

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