Variant report

Variant	nsv441979
Chromosome Location	chr5:178729588-178931306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1496)
CpG islands
(count:4400)
Chromatin interactive
region (count:63)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1496 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178921008-178921368	K562	blood:	n/a	n/a
2	ARID3A	chr5:178920984-178921396	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178931255-178932227	HepG2	liver:	n/a	n/a
4	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
5	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
7	BACH1	chr5:178782018-178782023	K562	blood:	n/a	n/a
8	BACH1	chr5:178770779-178771405	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:178753623-178753861	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:178867641-178867777	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
12	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
13	BHLHE40	chr5:178868515-178868770	K562	blood:	n/a	chr5:178868635-178868644 chr5:178868636-178868645 chr5:178868634-178868647 chr5:178868630-178868651 chr5:178868636-178868645 chr5:178868637-178868646
14	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
15	BHLHE40	chr5:178800328-178800428	K562	blood:	n/a	n/a
16	BHLHE40	chr5:178867642-178867915	K562	blood:	n/a	chr5:178867741-178867750 chr5:178867742-178867751 chr5:178867742-178867751 chr5:178867743-178867752 chr5:178867736-178867757 chr5:178867740-178867753
17	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr5:178826992-178827587	K562	blood:	n/a	n/a
19	CBX3	chr5:178820032-178820533	HCT-116	colon:	n/a	n/a
20	CBX3	chr5:178882860-178883255	K562	blood:	n/a	n/a
21	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
22	CBX3	chr5:178827067-178827261	K562	blood:	n/a	n/a
23	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
24	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
25	CEBPB	chr5:178783646-178783964	Hela-S3	cervix:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
26	CEBPB	chr5:178783645-178783928	A549	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
27	CEBPB	chr5:178918772-178918946	K562	blood:	n/a	chr5:178918811-178918822
28	CEBPB	chr5:178901825-178902196	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr5:178734831-178734994	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:178783581-178783974	IMR90	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
31	CEBPB	chr5:178731436-178731883	IMR90	lung:	n/a	n/a
32	CEBPB	chr5:178901823-178902191	MCF-7	breast:	n/a	n/a
33	CEBPB	chr5:178913744-178914042	IMR90	lung:	n/a	chr5:178913860-178913871
34	CEBPB	chr5:178920783-178920906	K562	blood:	n/a	n/a
35	CEBPB	chr5:178749384-178749670	IMR90	lung:	n/a	n/a
36	CEBPB	chr5:178819935-178820575	HCT-116	colon:	n/a	n/a
37	CEBPB	chr5:178901832-178902156	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:178819993-178820453	IMR90	lung:	n/a	n/a
39	CEBPB	chr5:178780036-178780236	IMR90	lung:	n/a	n/a
40	CEBPB	chr5:178898795-178899125	HepG2	liver:	n/a	n/a
41	CEBPB	chr5:178858362-178858799	MCF-7	breast:	n/a	n/a
42	CEBPB	chr5:178858449-178858788	HepG2	liver:	n/a	n/a
43	CEBPB	chr5:178858452-178858788	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr5:178786162-178786480	Hela-S3	cervix:	n/a	chr5:178786328-178786339
45	CEBPB	chr5:178901817-178902203	MCF-7	breast:	n/a	n/a
46	CEBPB	chr5:178858441-178858825	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr5:178901844-178902195	ECC-1	luminal epithelium:	n/a	n/a
48	CEBPB	chr5:178858431-178858818	A549	lung:	n/a	n/a
49	CEBPB	chr5:178791997-178792197	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:178898880-178899073	MCF-7	breast:	n/a	n/a

(count:4400 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178854202-178854252	HRCEpiC	kidney:	n/a
2	chr5:178753803-178753853	BE2_C	brain:	n/a
3	chr5:178772372-178772422	GM12891	blood:	n/a
4	chr5:178759017-178759067	CMK	blood:	n/a
5	chr5:178736443-178736493	U87	brain:	n/a
6	chr5:178767472-178767522	SK-N-SH	brain:	n/a
7	chr5:178773355-178773405	HRE	kidney:	n/a
8	chr5:178753803-178753853	HRPEpiC	eye:	n/a
9	chr5:178854202-178854252	HRCEpiC	kidney:	n/a
10	chr5:178753803-178753853	BE2_C	brain:	n/a
11	chr5:178772372-178772422	GM12891	blood:	n/a
12	chr5:178759017-178759067	CMK	blood:	n/a
13	chr5:178736443-178736493	U87	brain:	n/a
14	chr5:178767472-178767522	SK-N-SH	brain:	n/a
15	chr5:178773355-178773405	HRE	kidney:	n/a
16	chr5:178753803-178753853	HRPEpiC	eye:	n/a
17	chr5:178854202-178854252	AG04450	lung:	fetal
18	chr5:178913683-178913733	HCT-116	colon:	n/a
19	chr5:178800355-178800405	A549	lung:	n/a
20	chr5:178801500-178801550	IMR90	lung:	fetal
21	chr5:178854586-178854636	HRPEpiC	eye:	n/a
22	chr5:178800278-178800328	PANC-1	pancreas:	n/a
23	chr5:178773355-178773405	Hepatocyte	liver:	n/a
24	chr5:178741283-178741333	HNPCEpiC	eye:	n/a
25	chr5:178772390-178772440	MCF10A-Er-Src	breast:	n/a
26	chr5:178763419-178763469	MCF-7	breast:	n/a
27	chr5:178771776-178771826	GM12878	blood:	n/a
28	chr5:178803207-178803257	PrEC	prostate:	n/a
29	chr5:178801332-178801382	ovcar-3	ovarian:	n/a
30	chr5:178771329-178771379	H1-hESC	embryonic stem cell:	embryo
31	chr5:178899850-178899900	HCPEpiC	choroid plexus:	n/a
32	chr5:178803207-178803257	LNCaP	prostate:	n/a
33	chr5:178741205-178741255	SK-N-SH	brain:	n/a
34	chr5:178800355-178800405	LNCaP	prostate:	n/a
35	chr5:178748193-178748243	LNCaP	prostate:	n/a
36	chr5:178800278-178800328	ProgFib	skin:	n/a
37	chr5:178846740-178846790	HL-60	blood:	n/a
38	chr5:178789651-178789701	HUVEC	blood vessel:	n/a
39	chr5:178808997-178809047	PANC-1	pancreas:	n/a
40	chr5:178772390-178772440	SK-N-SH_RA	brain:	n/a
41	chr5:178741004-178741054	ProgFib	skin:	n/a
42	chr5:178735241-178735291	SK-N-SH_RA	brain:	n/a
43	chr5:178835943-178835993	NH-A	brain:	n/a
44	chr5:178772203-178772253	H1-hESC	embryonic stem cell:	embryo
45	chr5:178767472-178767522	U87	brain:	n/a
46	chr5:178902790-178902840	GM19239	blood:	n/a
47	chr5:178835943-178835993	AG09309	skin:	n/a
48	chr5:178735372-178735422	AG04450	lung:	fetal
49	chr5:178846740-178846790	RPTEC	kidney:	n/a
50	chr5:178763419-178763469	HMEC	breast:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
2	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
3	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
4	chr5:178905653..178907978-chr5:178976399..178978448,2	MCF-7	breast:
5	chr5:178892938..178894678-chr5:178896634..178898137,2	K562	blood:
6	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
7	chr5:178219922..178220838-chr5:178920668..178921270,2	MCF-7	breast:
8	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
9	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
10	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
11	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
12	chr5:178882272..178884920-chr5:179049238..179052060,2	K562	blood:
13	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
14	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
15	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
16	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
17	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
18	chr5:178219841..178220793-chr5:178920740..178921735,2	MCF-7	breast:
19	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
20	chr5:178688082..178688899-chr5:178920410..178921212,2	MCF-7	breast:
21	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
22	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
23	chr5:178815571..178817876-chr5:178818215..178820763,3	MCF-7	breast:
24	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
25	chr5:178594236..178594749-chr5:178920299..178921066,2	K562	blood:
26	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
27	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
28	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
29	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
30	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
31	chr5:178593773..178595177-chr5:178920715..178921686,6	MCF-7	breast:
32	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
33	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
34	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
35	chr5:178921207..178921791-chr5:179095335..179095939,2	K562	blood:
36	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
37	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
38	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
39	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
40	chr5:178923732..178926017-chr5:178977562..178979960,2	MCF-7	breast:
41	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
42	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
43	chr5:178815571..178817876-chr5:178818215..178820763,3	MCF-7	breast:
44	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
45	chr5:177708522..177710701-chr5:178921263..178923252,2	K562	blood:
46	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
47	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
48	chr12:72186780..72187498-chr5:178846162..178846680,2	MCF-7	breast:
49	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
50	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUFY1-1	chr5:178882416-178882818	XLOC_004674
2	lnc-RUFY1-2	chr5:178805707-178805866	ENSG00000253979
3	lnc-RUFY1-5	chr5:178815798-178815892	l_3076_chr5:178815797-178817202_testes
4	lnc-RUFY1-2	chr5:178804506-178804705	ENSG00000253979
5	lnc-ADAMTS2-2	chr5:178893834-178894126	NONHSAT105584
6	lnc-RUFY1-1	chr5:178882939-178883096	XLOC_004674
7	lnc-ADAMTS2-1	chr5:178805537-178805760	XLOC_005105
8	lnc-RUFY1-5	chr5:178816320-178816597	l_3076_chr5:178815797-178817202_testes
9	lnc-ADAMTS2-1	chr5:178804601-178804929	XLOC_005105
10	lnc-RUFY1-5	chr5:178816913-178817202	l_3076_chr5:178815797-178817202_testes
11	lnc-HNRNPH1-3	chr5:178930323-178930741	ENSG00000253652

No data

Variant related genes	Relation type
ENSG00000253163	TF binding region
ADAMTS2	TF binding region
ENSG00000253979	TF binding region
ENSG00000250674	TF binding region
RN7SL71P	TF binding region
ENSG00000253617	TF binding region
ENSG00000253163	CpG island
ADAMTS2	CpG island
ENSG00000253979	CpG island
ENSG00000250674	CpG island
RN7SL71P	CpG island
ENSG00000253617	CpG island
ENSG00000176783	chromatin interactions
ENSG00000264205	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000253617	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000253163	chromatin interactions
ENSG00000250674	chromatin interactions

Extended variants
information (count: 8750 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:8750 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557172941	chr5:178729603-178729604	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs199873301	chr5:178729640-178729641	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs181904677	chr5:178729641-178729642	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs569007303	chr5:178729646-178729647	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs184679899	chr5:178729692-178729693	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs573207401	chr5:178729697-178729698	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs540239121	chr5:178729703-178729704	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs558892366	chr5:178729727-178729728	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs577452211	chr5:178729732-178729733	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs544712119	chr5:178729734-178729735	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs562673303	chr5:178729752-178729753	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs539129078	chr5:178729792-178729793	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs529871911	chr5:178729805-178729806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542121355	chr5:178729852-178729853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560159011	chr5:178729853-178729854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527560115	chr5:178729869-178729870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551919939	chr5:178729877-178729878	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368748907	chr5:178729931-178729932	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570103485	chr5:178729932-178729933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189911294	chr5:178729936-178729937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181424997	chr5:178729963-178729964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141119657	chr5:178729968-178729969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs60490138	chr5:178729982-178729983	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs569118713	chr5:178729983-178729984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191035403	chr5:178729984-178729985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555267026	chr5:178729995-178729996	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10464054	chr5:178730017-178730018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567081877	chr5:178730035-178730036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2431423	chr5:178730062-178730063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528776922	chr5:178730079-178730080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs13185260	chr5:178730093-178730094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577261151	chr5:178730094-178730095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544724610	chr5:178730268-178730269	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs556658795	chr5:178730269-178730270	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs185038725	chr5:178730276-178730277	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs191022325	chr5:178730320-178730321	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs560279528	chr5:178730324-178730325	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs371025872	chr5:178730380-178730381	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs572291210	chr5:178730400-178730401	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs183161445	chr5:178730403-178730404	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs563742467	chr5:178730416-178730417	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs535397355	chr5:178730421-178730422	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs531169976	chr5:178730441-178730442	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs555237276	chr5:178730464-178730465	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs561420695	chr5:178730484-178730485	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs528963634	chr5:178730504-178730505	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs548535714	chr5:178730532-178730533	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs567048036	chr5:178730536-178730537	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs565590478	chr5:178730591-178730592	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs2450197	chr5:178730638-178730639	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:2103 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178716200-178730800	Weak transcription	HSMM	muscle
2	chr5:178723000-178730200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:178724400-178733600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:178725000-178729600	Weak transcription	Right Atrium	heart
5	chr5:178727000-178729800	Enhancers	Fetal Muscle Leg	muscle
6	chr5:178727200-178730200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr5:178727200-178731000	Enhancers	NHLF	lung
8	chr5:178727400-178730600	Enhancers	Placenta	Placenta
9	chr5:178727400-178731600	Enhancers	Adipose Nuclei	Adipose
10	chr5:178727400-178732600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr5:178727800-178730400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr5:178728000-178730800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr5:178728000-178730800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr5:178728000-178731200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:178728000-178741000	Weak transcription	Stomach Smooth Muscle	stomach
16	chr5:178728200-178730600	Enhancers	Osteobl	bone
17	chr5:178728400-178729600	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr5:178728400-178729800	Enhancers	Spleen	Spleen
19	chr5:178728600-178729600	Weak transcription	NHDF-Ad	bronchial
20	chr5:178728600-178730000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr5:178728600-178730200	Enhancers	Fetal Muscle Trunk	muscle
22	chr5:178728600-178730600	Enhancers	Lung	lung
23	chr5:178728800-178731200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:178729000-178729600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr5:178729000-178730000	Weak transcription	Fetal Lung	lung
26	chr5:178729000-178732000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:178729200-178729600	Weak transcription	Fetal Stomach	stomach
28	chr5:178729200-178741000	Weak transcription	Ovary	ovary
29	chr5:178729600-178729800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
30	chr5:178729600-178729800	Enhancers	Fetal Stomach	stomach
31	chr5:178729600-178729800	Enhancers	Gastric	stomach
32	chr5:178729600-178730200	Enhancers	Right Atrium	heart
33	chr5:178729600-178731000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr5:178729600-178731200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr5:178729600-178733200	Enhancers	NHDF-Ad	bronchial
36	chr5:178729800-178730200	Weak transcription	Fetal Stomach	stomach
37	chr5:178729800-178730800	Weak transcription	Gastric	stomach
38	chr5:178730000-178731000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:178730000-178731200	Enhancers	Fetal Lung	lung
40	chr5:178730200-178730400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr5:178730200-178730400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:178730200-178730600	Enhancers	Placenta Amnion	Placenta Amnion
43	chr5:178730200-178730600	Weak transcription	Right Atrium	heart
44	chr5:178730200-178730800	Weak transcription	Fetal Muscle Trunk	muscle
45	chr5:178730200-178731200	ZNF genes & repeats	Fetal Stomach	stomach
46	chr5:178730200-178731200	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr5:178730400-178730800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr5:178730400-178731200	Enhancers	HSMMtube	muscle
49	chr5:178730400-178731600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:178730600-178731000	Bivalent Enhancer	Placenta	Placenta

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