Variant report

Variant	nsv1003585
Chromosome Location	chr4:86957967-87250436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1347)
CpG islands
(count:550)
Chromatin interactive
region (count:50)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:87029865-87030369	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:86965091-86965502	K562	blood:	n/a	n/a
3	ARID3A	chr4:87144744-87144944	HepG2	liver:	n/a	n/a
4	ATF3	chr4:87144617-87145050	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:86997741-86997912	K562	blood:	n/a	n/a
6	BATF	chr4:87164990-87165297	GM12878	blood:	n/a	n/a
7	BATF	chr4:87164474-87164694	GM12878	blood:	n/a	n/a
8	BATF	chr4:87164975-87165324	GM12878	blood:	n/a	n/a
9	BCL3	chr4:87141044-87141632	A549	lung:	n/a	n/a
10	BCL3	chr4:87139848-87140698	A549	lung:	n/a	n/a
11	BHLHE40	chr4:87165152-87165200	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:87178519-87178786	K562	blood:	n/a	chr4:87178614-87178627 chr4:87178610-87178631 chr4:87178615-87178624
13	BHLHE40	chr4:87216133-87216356	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:87148090-87148128	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:87030030-87030251	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:87020633-87020671	K562	blood:	n/a	n/a
17	BRCA1	chr4:87216431-87216494	GM12878	blood:	n/a	n/a
18	BRCA1	chr4:87141061-87141619	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr4:87003832-87004143	K562	blood:	n/a	n/a
20	CEBPB	chr4:86957865-86958203	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:87233691-87233724	HepG2	liver:	n/a	chr4:87233695-87233706
22	CEBPB	chr4:87119485-87119620	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:87011200-87011377	K562	blood:	n/a	n/a
24	CEBPB	chr4:87063544-87063833	A549	lung:	n/a	chr4:87063684-87063695
25	CEBPB	chr4:87013911-87014575	K562	blood:	n/a	n/a
26	CEBPB	chr4:87039044-87039507	A549	lung:	n/a	n/a
27	CEBPB	chr4:87139832-87140652	Hela-S3	cervix:	n/a	chr4:87140416-87140427 chr4:87140418-87140429
28	CEBPB	chr4:87011160-87011360	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:87014294-87014539	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr4:87141385-87141611	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:87063517-87063828	IMR90	lung:	n/a	chr4:87063684-87063695
32	CEBPB	chr4:87011114-87011427	IMR90	lung:	n/a	n/a
33	CEBPB	chr4:87141290-87141719	A549	lung:	n/a	n/a
34	CEBPB	chr4:87014247-87014568	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:86965198-86965467	K562	blood:	n/a	n/a
36	CEBPB	chr4:87108365-87108678	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:87140149-87140547	MCF-7	breast:	n/a	chr4:87140416-87140427 chr4:87140418-87140429
38	CEBPB	chr4:87013871-87014555	A549	lung:	n/a	n/a
39	CEBPB	chr4:87063561-87063863	K562	blood:	n/a	chr4:87063684-87063695
40	CEBPB	chr4:87141356-87141683	A549	lung:	n/a	n/a
41	CEBPB	chr4:87140175-87140643	A549	lung:	n/a	chr4:87140416-87140427 chr4:87140418-87140429
42	CEBPB	chr4:87140962-87141783	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:87178489-87178610	K562	blood:	n/a	n/a
44	CEBPB	chr4:87108462-87108618	A549	lung:	n/a	n/a
45	CEBPB	chr4:87011178-87011337	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr4:87212095-87212119	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr4:87140239-87140583	IMR90	lung:	n/a	chr4:87140416-87140427 chr4:87140418-87140429
48	CEBPB	chr4:87105460-87105731	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:86965182-86965455	A549	lung:	n/a	n/a
50	CEBPB	chr4:87140179-87140660	A549	lung:	n/a	chr4:87140416-87140427 chr4:87140418-87140429

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:87230737-87230787	AG10803	skin:	n/a
2	chr4:87230737-87230787	AG10803	skin:	n/a
3	chr4:87030123-87030173	AG04450	lung:	fetal
4	chr4:87230737-87230787	HCPEpiC	choroid plexus:	n/a
5	chr4:87235054-87235104	HUVEC	blood vessel:	n/a
6	chr4:87040423-87040473	A549	lung:	n/a
7	chr4:87230737-87230787	HMEC	breast:	n/a
8	chr4:87040423-87040473	AG09319	gingival:	n/a
9	chr4:86997288-86997338	HCPEpiC	choroid plexus:	n/a
10	chr4:86997288-86997338	ECC-1	luminal epithelium:	n/a
11	chr4:87040423-87040473	PrEC	prostate:	n/a
12	chr4:87187259-87187309	U87	brain:	n/a
13	chr4:87230737-87230787	SKMC	muscle:	n/a
14	chr4:87230737-87230787	HRCEpiC	kidney:	n/a
15	chr4:87030123-87030173	MCF10A-Er-Src	breast:	n/a
16	chr4:86997288-86997338	SK-N-MC	brain:	n/a
17	chr4:87028602-87028652	HUVEC	blood vessel:	n/a
18	chr4:87187259-87187309	HCF	heart:	n/a
19	chr4:86997288-86997338	A549	lung:	n/a
20	chr4:87040423-87040473	Hela-S3	cervix:	n/a
21	chr4:86997288-86997338	NH-A	brain:	n/a
22	chr4:87187259-87187309	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:87230737-87230787	NT2-D1	testis:	n/a
24	chr4:86997288-86997338	HRCEpiC	kidney:	n/a
25	chr4:87187259-87187309	CMK	blood:	n/a
26	chr4:87187259-87187309	HEEpiC	esophagus:	n/a
27	chr4:87235054-87235104	AoSMC	blood vessel:	n/a
28	chr4:87230737-87230787	HL-60	blood:	n/a
29	chr4:87235054-87235104	IMR90	lung:	fetal
30	chr4:87040423-87040473	SK-N-MC	brain:	n/a
31	chr4:87230737-87230787	U87	brain:	n/a
32	chr4:87230737-87230787	ovcar-3	ovarian:	n/a
33	chr4:87235054-87235104	GM12878	blood:	n/a
34	chr4:87028602-87028652	T-47D	breast:	n/a
35	chr4:87030123-87030173	NB4	blood:	n/a
36	chr4:87235054-87235104	CMK	blood:	n/a
37	chr4:87235054-87235104	U87	brain:	n/a
38	chr4:87028501-87028551	SAEC	small airway:	n/a
39	chr4:87235054-87235104	SK-N-SH	brain:	n/a
40	chr4:87030123-87030173	HRPEpiC	eye:	n/a
41	chr4:87187259-87187309	GM12891	blood:	n/a
42	chr4:87040423-87040473	GM19239	blood:	n/a
43	chr4:87040423-87040473	IMR90	lung:	fetal
44	chr4:87056153-87056203	HEEpiC	esophagus:	n/a
45	chr4:87187259-87187309	T-47D	breast:	n/a
46	chr4:87235054-87235104	MCF-7	breast:	n/a
47	chr4:87040423-87040473	GM12891	blood:	n/a
48	chr4:87028602-87028652	SK-N-SH	brain:	n/a
49	chr4:87028602-87028652	AG09319	gingival:	n/a
50	chr4:87187259-87187309	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:86996153..86999257-chr4:86999314..87002749,3	K562	blood:
2	chr4:86974348..86976679-chr4:86978244..86980026,2	MCF-7	breast:
3	chr4:87068101..87070840-chr4:87077987..87079819,2	MCF-7	breast:
4	chr4:87206946..87210135-chr4:87210716..87213882,3	K562	blood:
5	chr4:86728075..86730663-chr4:86957838..86959662,2	MCF-7	breast:
6	chr4:87132187..87133769-chr4:87135857..87137593,2	MCF-7	breast:
7	chr4:87155810..87157593-chr4:87170077..87172350,2	K562	blood:
8	chr4:87134159..87136485-chr4:87181961..87184950,2	MCF-7	breast:
9	chr4:86717637..86718454-chr4:86964866..86965718,3	MCF-7	breast:
10	chr4:86964897..86966021-chr4:87144762..87145373,4	MCF-7	breast:
11	chr4:87018345..87020243-chr4:87021552..87023121,2	MCF-7	breast:
12	chr4:87074554..87076995-chr4:87081060..87082909,2	MCF-7	breast:
13	chr4:87226178..87227870-chr4:87231793..87233350,2	MCF-7	breast:
14	chr4:87070864..87072590-chr4:87074186..87076954,2	K562	blood:
15	chr17:67196658..67197255-chr4:86998915..86999454,2	HCT-116	colon:
16	chr4:87195749..87198427-chr4:87210790..87213318,2	MCF-7	breast:
17	chr4:87188315..87191047-chr4:87191829..87193985,2	MCF-7	breast:
18	chr17:56708544..56709369-chr4:87190972..87191472,2	Hela-S3	cervix:
19	chr4:87074554..87076995-chr4:87081060..87082909,2	MCF-7	breast:
20	chr4:87132187..87133769-chr4:87135857..87137593,2	MCF-7	breast:
21	chr4:87070864..87073086-chr4:87075454..87077437,2	K562	blood:
22	chr4:87024355..87027343-chr4:87027765..87029282,2	MCF-7	breast:
23	chr4:87183674..87187410-chr4:87190409..87192720,3	K562	blood:
24	chr4:87070864..87072590-chr4:87074186..87076954,2	K562	blood:
25	chr4:86717526..86718413-chr4:86964881..86965596,2	MCF-7	breast:
26	chr4:87140077..87142353-chr4:87143339..87145832,2	MCF-7	breast:
27	chr4:87134159..87136485-chr4:87181961..87184950,2	MCF-7	breast:
28	chr4:87048655..87051037-chr4:87083679..87085994,2	MCF-7	breast:
29	chr4:87079015..87081853-chr4:87083542..87085468,2	K562	blood:
30	chr4:87183674..87187410-chr4:87190409..87192720,3	K562	blood:
31	chr4:87195749..87198427-chr4:87210790..87213318,2	MCF-7	breast:
32	chr4:86964897..86966021-chr4:87144762..87145373,4	MCF-7	breast:
33	chr4:86974348..86976679-chr4:86978244..86980026,2	MCF-7	breast:
34	chr4:87179144..87180691-chr4:87183736..87185339,2	K562	blood:
35	chr4:87188315..87191047-chr4:87191829..87193985,2	MCF-7	breast:
36	chr4:87079015..87081853-chr4:87083542..87085468,2	K562	blood:
37	chr4:87118979..87120763-chr4:87124229..87126055,2	K562	blood:
38	chr4:87155810..87157593-chr4:87170077..87172350,2	K562	blood:
39	chr4:87024355..87027343-chr4:87027765..87029282,2	MCF-7	breast:
40	chr4:87179144..87180691-chr4:87183736..87185339,2	K562	blood:
41	chr4:87070864..87073086-chr4:87075454..87077437,2	K562	blood:
42	chr4:87140077..87142353-chr4:87143339..87145832,2	MCF-7	breast:
43	chr4:86996065..86997848-chr4:87003738..87005825,2	K562	blood:
44	chr4:87226178..87227870-chr4:87231793..87233350,2	MCF-7	breast:
45	chr4:87118979..87120763-chr4:87124229..87126055,2	K562	blood:
46	chr4:86996065..86997848-chr4:87003738..87005825,2	K562	blood:
47	chr4:86996153..86999257-chr4:86999314..87002749,3	K562	blood:
48	chr4:87206946..87210135-chr4:87210716..87213882,3	K562	blood:
49	chr4:87068101..87070840-chr4:87077987..87079819,2	MCF-7	breast:
50	chr4:87048655..87051037-chr4:87083679..87085994,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP24-1	chr4:87041137-87041754	ENSG00000250062.1
2	lnc-ARHGAP24-1	chr4:87039065-87039115	ENSG00000250062.1
3	lnc-ARHGAP24-1	chr4:87041137-87041754	NONHSAT097275
4	lnc-ARHGAP24-1	chr4:87048745-87048853	ENSG00000250062.1
5	lnc-ARHGAP24-1	chr4:87040879-87041036	NONHSAT097275
6	lnc-ARHGAP24-1	chr4:87041137-87041754	ENSG00000250062.1
7	lnc-ARHGAP24-1	chr4:87040867-87041036	ENSG00000250062.1
8	lnc-SLC10A6-4	chr4:87097140-87097232	NONHSAT097276
9	lnc-SLC10A6-4	chr4:87085599-87085718	NONHSAT097276
10	lnc-ARHGAP24-1	chr4:87048745-87048841	ENSG00000250062.1
11	lnc-SLC10A6-4	chr4:87115489-87115560	NONHSAT097276
12	lnc-SLC10A6-4	chr4:87221733-87222013	NONHSAT097277
13	lnc-ARHGAP24-1	chr4:87048745-87048940	NONHSAT097275
14	lnc-ARHGAP24-1	chr4:87140928-87141079	ENSG00000250062.1

No data

Variant related genes	Relation type
MAPK10	TF binding region
ENSG00000250062	TF binding region
MAPK10	CpG island
ENSG00000250062	CpG island
ENSG00000109339	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 9783 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:9783 , 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	rs181361578	chr4:86957975-86957976	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185404611	chr4:86958011-86958012	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs562793727	chr4:86958046-86958047	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs189969099	chr4:86958057-86958058	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs551397759	chr4:86958103-86958104	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs566509342	chr4:86958124-86958125	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs376597629	chr4:86958195-86958196	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs182268813	chr4:86958211-86958212	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs73833997	chr4:86958213-86958214	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs567923534	chr4:86958224-86958225	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs150183390	chr4:86958228-86958229	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs143021927	chr4:86958230-86958231	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs147308609	chr4:86958231-86958232	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs184886665	chr4:86958242-86958243	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs550749720	chr4:86958279-86958280	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs141171916	chr4:86958321-86958322	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs200787570	chr4:86958346-86958347	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs572779427	chr4:86958389-86958390	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs539501950	chr4:86958390-86958391	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs557812183	chr4:86958469-86958470	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572846093	chr4:86958470-86958471	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534511142	chr4:86958491-86958492	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556055197	chr4:86958505-86958506	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574179832	chr4:86958523-86958524	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544521087	chr4:86958530-86958531	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35755826	chr4:86958576-86958577	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs578054841	chr4:86958608-86958609	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs58836254	chr4:86958685-86958686	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13353771	chr4:86958694-86958695	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs560133503	chr4:86958768-86958769	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372528038	chr4:86958800-86958801	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533243886	chr4:86958824-86958825	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs527641419	chr4:86958890-86958891	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546494712	chr4:86958897-86958898	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561882360	chr4:86958902-86958903	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs66850367	chr4:86958912-86958913	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs550534846	chr4:86958964-86958965	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78642606	chr4:86959210-86959211	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544081536	chr4:86959243-86959244	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539559136	chr4:86959282-86959283	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545353876	chr4:86959310-86959311	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs80336668	chr4:86959321-86959322	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116296798	chr4:86959356-86959357	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191054621	chr4:86959414-86959415	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555398082	chr4:86959565-86959566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184041258	chr4:86959570-86959571	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538510488	chr4:86959575-86959576	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556502490	chr4:86959588-86959589	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76063305	chr4:86959613-86959614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111302006	chr4:86959629-86959630	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
lymphocytic leukemia	21291569	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
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	20459617	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1452 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86916800-86985400	Weak transcription	Ovary	ovary
2	chr4:86936000-86975600	Weak transcription	Brain Germinal Matrix	brain
3	chr4:86936400-86990600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr4:86944600-86963000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:86945400-86963200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:86948200-86966600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:86949200-86988600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr4:86950600-86959200	Weak transcription	Fetal Brain Male	brain
9	chr4:86950600-86967000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr4:86953800-86959600	Enhancers	HUVEC	blood vessel
11	chr4:86954600-86958400	Enhancers	Osteobl	bone
12	chr4:86954600-86959000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr4:86954600-86960400	Weak transcription	Pancreas	Pancrea
14	chr4:86954600-86960600	Weak transcription	Left Ventricle	heart
15	chr4:86954800-86959000	Weak transcription	Fetal Lung	lung
16	chr4:86954800-86960400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:86955000-86958000	Weak transcription	Hela-S3	cervix
18	chr4:86955000-86958200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr4:86955000-86959200	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr4:86955000-86960400	Weak transcription	Fetal Stomach	stomach
21	chr4:86955000-86964400	Weak transcription	Brain Anterior Caudate	brain
22	chr4:86955000-86966400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:86955000-86985000	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr4:86955200-86960200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr4:86955200-86962600	Weak transcription	Aorta	Aorta
26	chr4:86955200-86964400	Weak transcription	Brain Substantia Nigra	brain
27	chr4:86955200-86964800	Weak transcription	Brain Angular Gyrus	brain
28	chr4:86955200-86965000	Weak transcription	Right Atrium	heart
29	chr4:86955200-86966600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr4:86955200-86971000	Weak transcription	Brain Hippocampus Middle	brain
31	chr4:86955200-87003800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr4:86955600-86963000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:86956000-86958200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr4:86956000-86958400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:86956200-86969600	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr4:86956600-86958800	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr4:86956800-86958000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:86956800-86958000	Enhancers	NH-A	brain
39	chr4:86956800-86958000	Enhancers	NHLF	lung
40	chr4:86956800-86958200	Enhancers	NHEK	skin
41	chr4:86956800-86958400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr4:86956800-86958400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:86956800-86958400	Enhancers	HMEC	breast
44	chr4:86956800-86960000	Enhancers	Fetal Heart	heart
45	chr4:86957000-86958200	Enhancers	Primary T cells from cord blood	blood
46	chr4:86957000-86958400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:86957000-86958400	Enhancers	Primary hematopoietic stem cells	blood
48	chr4:86957200-86958400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:86957800-86958200	Enhancers	Fetal Brain Female	brain
50	chr4:86957800-86958200	Enhancers	HSMMtube	muscle

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