Variant report

Variant	nsv882388
Chromosome Location	chr5:94764006-94925849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1165)
CpG islands
(count:1527)
Chromatin interactive
region (count:90)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:94829849-94829850	K562	blood:	n/a	n/a
2	ARID3A	chr5:94889972-94891319	K562	blood:	n/a	chr5:94890748-94890764 chr5:94890749-94890765
3	ARID3A	chr5:94890324-94891666	HepG2	liver:	n/a	chr5:94890748-94890764 chr5:94890749-94890765
4	ARID3A	chr5:94919516-94920080	K562	blood:	n/a	n/a
5	ARID3A	chr5:94781838-94781931	K562	blood:	n/a	n/a
6	ARID3A	chr5:94777839-94777887	HepG2	liver:	n/a	n/a
7	ATF1	chr5:94899136-94899384	K562	blood:	n/a	n/a
8	ATF1	chr5:94890036-94891154	K562	blood:	n/a	n/a
9	ATF1	chr5:94781761-94782087	K562	blood:	n/a	n/a
10	ATF2	chr5:94890405-94890937	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr5:94890108-94891163	GM12878	blood:	n/a	n/a
12	ATF2	chr5:94890406-94890866	GM12878	blood:	n/a	n/a
13	ATF3	chr5:94890488-94891027	A549	lung:	n/a	chr5:94890711-94890720
14	ATF3	chr5:94890443-94891024	HepG2	liver:	n/a	chr5:94890711-94890720
15	ATF3	chr5:94890559-94890903	K562	blood:	n/a	chr5:94890711-94890720
16	ATF3	chr5:94890493-94891026	GM12878	blood:	n/a	chr5:94890711-94890720
17	BACH1	chr5:94783398-94783516	K562	blood:	n/a	n/a
18	BACH1	chr5:94808083-94808164	K562	blood:	n/a	n/a
19	BACH1	chr5:94890187-94890866	K562	blood:	n/a	n/a
20	BACH1	chr5:94879068-94879199	K562	blood:	n/a	n/a
21	BATF	chr5:94868842-94869040	GM12878	blood:	n/a	chr5:94868843-94868852 chr5:94868925-94868936
22	BCL3	chr5:94890326-94891150	A549	lung:	n/a	n/a
23	BCLAF1	chr5:94889983-94891302	GM12878	blood:	n/a	chr5:94891161-94891170 chr5:94890288-94890301
24	BCLAF1	chr5:94890067-94891365	GM12878	blood:	n/a	chr5:94891161-94891170 chr5:94890288-94890301
25	BHLHE40	chr5:94890518-94890969	HepG2	liver:	n/a	chr5:94890712-94890721 chr5:94890711-94890720 chr5:94890705-94890726
26	BHLHE40	chr5:94890064-94891428	K562	blood:	n/a	chr5:94890712-94890721 chr5:94890711-94890720 chr5:94890705-94890726
27	BHLHE40	chr5:94890159-94891408	GM12878	blood:	n/a	chr5:94890712-94890721 chr5:94890711-94890720 chr5:94890705-94890726
28	BHLHE40	chr5:94890571-94890856	HepG2	liver:	n/a	chr5:94890712-94890721 chr5:94890711-94890720 chr5:94890705-94890726
29	BHLHE40	chr5:94889422-94889832	K562	blood:	n/a	n/a
30	BHLHE40	chr5:94890539-94890928	A549	lung:	n/a	chr5:94890712-94890721 chr5:94890711-94890720 chr5:94890705-94890726
31	BHLHE40	chr5:94890316-94891233	HepG2	liver:	n/a	chr5:94890712-94890721 chr5:94890711-94890720 chr5:94890705-94890726
32	BRCA1	chr5:94889537-94889789	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr5:94890389-94891192	GM12878	blood:	n/a	n/a
34	BRCA1	chr5:94890112-94892024	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr5:94890373-94891243	HepG2	liver:	n/a	n/a
36	BRCA1	chr5:94864243-94864397	Hela-S3	cervix:	n/a	n/a
37	CBX3	chr5:94823592-94823950	K562	blood:	n/a	n/a
38	CBX3	chr5:94890524-94890975	K562	blood:	n/a	n/a
39	CBX3	chr5:94890058-94891328	K562	blood:	n/a	n/a
40	CBX3	chr5:94823566-94823944	HCT-116	colon:	n/a	n/a
41	CCNT2	chr5:94889430-94889659	K562	blood:	n/a	n/a
42	CCNT2	chr5:94890002-94891335	K562	blood:	n/a	chr5:94891125-94891134 chr5:94890553-94890562
43	CCNT2	chr5:94899183-94899383	K562	blood:	n/a	n/a
44	CCNT2	chr5:94902108-94902191	K562	blood:	n/a	n/a
45	CCNT2	chr5:94878848-94879367	K562	blood:	n/a	n/a
46	CCNT2	chr5:94919637-94920093	K562	blood:	n/a	n/a
47	CEBPB	chr5:94785526-94785688	A549	lung:	n/a	chr5:94785590-94785601 chr5:94785588-94785605 chr5:94785589-94785602 chr5:94785589-94785602 chr5:94785589-94785602 chr5:94785589-94785600 chr5:94785622-94785633 chr5:94785589-94785600
48	CEBPB	chr5:94775561-94776091	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr5:94785431-94785715	K562	blood:	n/a	chr5:94785590-94785601 chr5:94785588-94785605 chr5:94785589-94785602 chr5:94785589-94785602 chr5:94785589-94785602 chr5:94785589-94785600 chr5:94785622-94785633 chr5:94785589-94785600
50	CEBPB	chr5:94765676-94765697	A549	lung:	n/a	n/a

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:94890411-94890461	PrEC	prostate:	n/a
2	chr5:94891907-94891957	GM12878	blood:	n/a
3	chr5:94890411-94890461	PrEC	prostate:	n/a
4	chr5:94891907-94891957	GM12878	blood:	n/a
5	chr5:94891907-94891957	SK-N-SH_RA	brain:	n/a
6	chr5:94890687-94890737	HRCEpiC	kidney:	n/a
7	chr5:94890164-94890214	GM06990	blood:	n/a
8	chr5:94891907-94891957	SK-N-SH	brain:	n/a
9	chr5:94784489-94784539	Jurkat	blood:	n/a
10	chr5:94890687-94890737	PFSK-1	brain:	n/a
11	chr5:94890411-94890461	Hepatocyte	liver:	n/a
12	chr5:94890164-94890214	HRCEpiC	kidney:	n/a
13	chr5:94890855-94890905	H1-hESC	embryonic stem cell:	embryo
14	chr5:94890687-94890737	PrEC	prostate:	n/a
15	chr5:94890817-94890867	HEEpiC	esophagus:	n/a
16	chr5:94893759-94893809	HRCEpiC	kidney:	n/a
17	chr5:94891907-94891957	HMEC	breast:	n/a
18	chr5:94890164-94890214	SAEC	small airway:	n/a
19	chr5:94890897-94890947	GM19239	blood:	n/a
20	chr5:94891907-94891957	SK-N-MC	brain:	n/a
21	chr5:94890408-94890458	AG09309	skin:	n/a
22	chr5:94891907-94891957	HRE	kidney:	n/a
23	chr5:94890897-94890947	SAEC	small airway:	n/a
24	chr5:94891907-94891957	NH-A	brain:	n/a
25	chr5:94775923-94775973	SK-N-SH	brain:	n/a
26	chr5:94890810-94890860	AG04450	lung:	fetal
27	chr5:94879974-94880024	H1-hESC	embryonic stem cell:	embryo
28	chr5:94901279-94901329	HMEC	breast:	n/a
29	chr5:94890687-94890737	MCF10A-Er-Src	breast:	n/a
30	chr5:94890783-94890833	NH-A	brain:	n/a
31	chr5:94784489-94784539	HNPCEpiC	eye:	n/a
32	chr5:94890897-94890947	GM12891	blood:	n/a
33	chr5:94901279-94901329	U87	brain:	n/a
34	chr5:94893759-94893809	ovcar-3	ovarian:	n/a
35	chr5:94890715-94890765	GM06990	blood:	n/a
36	chr5:94887809-94887859	MCF-7	breast:	n/a
37	chr5:94890783-94890833	HL-60	blood:	n/a
38	chr5:94784489-94784539	NT2-D1	testis:	n/a
39	chr5:94890411-94890461	PFSK-1	brain:	n/a
40	chr5:94887809-94887859	SAEC	small airway:	n/a
41	chr5:94890852-94890902	HEEpiC	esophagus:	n/a
42	chr5:94890408-94890458	HAEpiC	amniotic membrane:	n/a
43	chr5:94891907-94891957	HCPEpiC	choroid plexus:	n/a
44	chr5:94890123-94890173	U87	brain:	n/a
45	chr5:94890715-94890765	HRE	kidney:	n/a
46	chr5:94890810-94890860	SKMC	muscle:	n/a
47	chr5:94890164-94890214	LNCaP	prostate:	n/a
48	chr5:94890667-94890717	NHDF-neo	bronchial:	n/a
49	chr5:94890687-94890737	HL-60	blood:	n/a
50	chr5:94890123-94890173	AoSMC	blood vessel:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:94779335..94782524-chr5:94785930..94789104,3	MCF-7	breast:
2	chr5:94889284..94894325-chr5:94922703..94926825,4	K562	blood:
3	chr5:94892921..94894446-chr5:94936701..94939146,2	K562	blood:
4	chr5:94889800..94892273-chr5:94955578..94957837,2	MCF-7	breast:
5	chr5:94890271..94892404-chr5:94906433..94908089,2	K562	blood:
6	chr5:94919209..94922731-chr5:94929530..94932607,3	K562	blood:
7	chr5:94792282..94794324-chr5:94798104..94800472,2	K562	blood:
8	chr5:94775142..94778090-chr5:94885546..94887301,2	K562	blood:
9	chr5:94797653..94799389-chr5:94800929..94802912,2	K562	blood:
10	chr5:94840762..94844216-chr5:94846022..94849276,5	K562	blood:
11	chr5:94895692..94898424-chr5:94902068..94903763,2	K562	blood:
12	chr5:94866250..94868865-chr5:94878722..94881259,2	K562	blood:
13	chr5:94890265..94891768-chr5:95158248..95160600,2	K562	blood:
14	chr5:94772779..94775634-chr5:94777609..94779631,2	K562	blood:
15	chr5:94854160..94855779-chr5:94859258..94861480,2	MCF-7	breast:
16	chr5:94869385..94872836-chr5:94884055..94887302,3	K562	blood:
17	chr5:94831708..94834724-chr5:94836211..94838681,3	K562	blood:
18	chr5:94827564..94830154-chr5:94864488..94867318,2	K562	blood:
19	chr5:94889931..94892481-chr5:94918189..94920315,3	K562	blood:
20	chr5:94774570..94777503-chr5:94779746..94783694,3	K562	blood:
21	chr5:94762392..94764718-chr5:94767557..94769883,2	K562	blood:
22	chr5:94910804..94914424-chr5:94915690..94919110,3	K562	blood:
23	chr5:94824257..94827228-chr5:94828970..94832558,4	K562	blood:
24	chr5:94791113..94793048-chr5:94801350..94803549,2	K562	blood:
25	chr5:94910804..94914424-chr5:94915690..94919110,3	K562	blood:
26	chr5:94792282..94796231-chr5:94797879..94800684,4	K562	blood:
27	chr5:94866250..94868865-chr5:94878722..94881259,2	K562	blood:
28	chr5:94787545..94789529-chr5:94790641..94792240,2	K562	blood:
29	chr5:94885887..94888055-chr5:94890822..94893309,3	K562	blood:
30	chr5:94885448..94888187-chr5:94888844..94890737,5	K562	blood:
31	chr5:94779335..94782524-chr5:94785930..94789104,3	MCF-7	breast:
32	chr5:94892616..94895050-chr5:95181504..95183040,2	MCF-7	breast:
33	chr5:94924450..94926952-chr5:94932627..94934367,2	K562	blood:
34	chr5:94831708..94834724-chr5:94836211..94838681,3	K562	blood:
35	chr5:94796017..94797723-chr5:94996114..94998277,2	K562	blood:
36	chr5:94830912..94834910-chr5:94838887..94842661,5	K562	blood:
37	chr5:94815715..94817542-chr5:94820797..94823312,2	K562	blood:
38	chr5:94835766..94839248-chr5:94841208..94845104,3	K562	blood:
39	chr5:94760378..94762574-chr5:94766108..94768067,2	K562	blood:
40	chr5:94907342..94909603-chr5:94913208..94915224,2	K562	blood:
41	chr5:94885887..94888055-chr5:94890822..94893309,3	K562	blood:
42	chr5:94822418..94825374-chr5:94981248..94983908,2	K562	blood:
43	chr5:94768780..94772017-chr5:94775443..94778339,3	K562	blood:
44	chr5:94768113..94770869-chr5:94781811..94784172,2	K562	blood:
45	chr5:94791113..94793048-chr5:94801350..94803549,2	K562	blood:
46	chr5:94772779..94775634-chr5:94777609..94779631,2	K562	blood:
47	chr5:94895692..94898424-chr5:94902068..94903763,2	K562	blood:
48	chr5:94789443..94791165-chr5:94792736..94794259,2	K562	blood:
49	chr5:94797653..94799389-chr5:94800929..94802912,2	K562	blood:
50	chr5:94889576..94892057-chr5:94893383..94894937,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPATA9-4	chr5:94863717-94863856	NONHSAT102848
2	lnc-FAM81B-2	chr5:94796941-94798112	NONHSAT102843
3	lnc-FAM81B-3	chr5:94798402-94799375	NONHSAT102844
4	lnc-SPATA9-4	chr5:94864705-94864806	NONHSAT102848
5	lnc-FAM81B-1	chr5:94796346-94796855	NONHSAT102842
6	lnc-SPATA9-4	chr5:94864971-94865065	NONHSAT102848

No data

Variant related genes	Relation type
ARSK	TF binding region
RNU6-308P	TF binding region
FAM81B	TF binding region
TTC37	TF binding region
ENSG00000225165	TF binding region
ARSK	CpG island
RNU6-308P	CpG island
FAM81B	CpG island
TTC37	CpG island
ENSG00000225165	CpG island
ENSG00000212259	chromatin interactions
ENSG00000164291	chromatin interactions
ENSG00000153347	chromatin interactions
ENSG00000198677	chromatin interactions
ENSG00000178015	chromatin interactions
ENSG00000153113	chromatin interactions
ENSG00000175449	chromatin interactions
ENSG00000225165	chromatin interactions
ENSG00000173221	chromatin interactions

Extended variants
information (count: 5386 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:5386 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188704135	chr5:94767604-94767605	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs576992148	chr5:94767609-94767610	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs144147818	chr5:94767640-94767641	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181678930	chr5:94767669-94767670	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs116037259	chr5:94767706-94767707	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs561791123	chr5:94767731-94767732	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs530858029	chr5:94767780-94767781	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550465556	chr5:94767823-94767824	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187088379	chr5:94767830-94767831	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73141949	chr5:94767831-94767832	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546713846	chr5:94767832-94767833	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375636365	chr5:94767916-94767917	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73778839	chr5:94767923-94767924	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs535400053	chr5:94767976-94767977	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147292683	chr5:94767980-94767981	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574998788	chr5:94767987-94767988	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs28491117	chr5:94768050-94768051	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs73141954	chr5:94768091-94768092	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs191874194	chr5:94768144-94768145	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560126499	chr5:94768161-94768162	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs559382460	chr5:94768237-94768238	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs184112867	chr5:94768275-94768276	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs573007223	chr5:94768277-94768278	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541795837	chr5:94768335-94768336	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200107293	chr5:94768350-94768351	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185159280	chr5:94768385-94768386	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530841959	chr5:94768413-94768414	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550827940	chr5:94768430-94768431	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs564267849	chr5:94768549-94768550	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs139915984	chr5:94768596-94768597	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs533150490	chr5:94768621-94768622	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs373905643	chr5:94768702-94768703	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs546825546	chr5:94768743-94768744	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs149828491	chr5:94768816-94768817	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs535566136	chr5:94768850-94768851	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs562257656	chr5:94768875-94768876	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs548840828	chr5:94768876-94768877	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs568813998	chr5:94768932-94768933	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs143931722	chr5:94768937-94768938	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs201371375	chr5:94768963-94768964	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs189864949	chr5:94768965-94768966	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs147959761	chr5:94768966-94768967	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs148638732	chr5:94768997-94768998	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539599206	chr5:94769029-94769030	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs142039728	chr5:94769123-94769124	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs7725419	chr5:94769159-94769160	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs182493328	chr5:94769201-94769202	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs115920191	chr5:94769232-94769233	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs116227819	chr5:94769302-94769303	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187131055	chr5:94769308-94769309	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3865 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94768600-94776000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:94770000-94770400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:94770200-94771000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:94770600-94771000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:94770600-94771000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr5:94770600-94771200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:94771200-94775600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:94771800-94772400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr5:94772400-94773400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:94773400-94775400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:94773600-94775600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr5:94773800-94774000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr5:94773800-94774000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr5:94773800-94774200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:94773800-94775200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:94773800-94775600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:94774000-94775600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr5:94774200-94775200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr5:94774200-94776200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr5:94774200-94776200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:94775000-94775600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr5:94775200-94775400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr5:94775200-94776000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
24	chr5:94775200-94776200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr5:94775400-94775600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr5:94775400-94775800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr5:94775600-94775800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr5:94775600-94775800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr5:94775600-94775800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:94775600-94776000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:94775600-94776000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:94775600-94776400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
33	chr5:94775600-94776600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr5:94775600-94776600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
35	chr5:94775600-94776800	Enhancers	H9 Cell Line	embryonic stem cell
36	chr5:94775800-94776000	Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr5:94775800-94776200	Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr5:94775800-94776200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:94775800-94776200	Bivalent Enhancer	Fetal Heart	heart
40	chr5:94775800-94776600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:94776000-94776200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:94776000-94776200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
43	chr5:94776000-94776400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr5:94776000-94776400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:94776000-94776600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr5:94776000-94776800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr5:94776200-94776400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr5:94776200-94776400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr5:94776200-94776600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
50	chr5:94776200-94776800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell

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