Variant report

Variant	nsv1018641
Chromosome Location	chr5:178627012-178911254
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2073)
CpG islands
(count:7331)
Chromatin interactive
region (count:92)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2073 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:178658394-178658571	K562	blood:	n/a	n/a
2	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
3	ATF2	chr5:178688256-178688623	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
6	BACH1	chr5:178867641-178867777	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:178688361-178688719	H1-hESC	embryonic stem cell:	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	chr5:178782018-178782023	K562	blood:	n/a	n/a
11	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
12	BCL3	chr5:178650528-178650927	GM12878	blood:	n/a	n/a
13	BCL3	chr5:178650193-178650886	GM12878	blood:	n/a	n/a
14	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
15	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
16	BHLHE40	chr5:178655800-178656133	K562	blood:	n/a	n/a
17	BHLHE40	chr5:178712032-178712059	K562	blood:	n/a	n/a
18	BHLHE40	chr5:178722893-178723057	K562	blood:	n/a	chr5:178723031-178723040 chr5:178723031-178723040
19	BHLHE40	chr5:178691705-178692905	HepG2	liver:	n/a	chr5:178692685-178692701 chr5:178692599-178692615
20	BHLHE40	chr5:178639943-178640216	K562	blood:	n/a	n/a
21	BHLHE40	chr5:178695327-178695745	HepG2	liver:	n/a	n/a
22	BHLHE40	chr5:178703446-178703646	K562	blood:	n/a	n/a
23	BHLHE40	chr5:178800328-178800428	K562	blood:	n/a	n/a
24	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
25	BHLHE40	chr5:178703014-178703214	K562	blood:	n/a	n/a
26	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
27	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr5:178827067-178827261	K562	blood:	n/a	n/a
29	CBX3	chr5:178820032-178820533	HCT-116	colon:	n/a	n/a
30	CBX3	chr5:178826992-178827587	K562	blood:	n/a	n/a
31	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
32	CBX3	chr5:178882860-178883255	K562	blood:	n/a	n/a
33	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
34	CCNT2	chr5:178702918-178703113	K562	blood:	n/a	n/a
35	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
36	CEBPB	chr5:178786289-178786460	HepG2	liver:	n/a	chr5:178786328-178786339
37	CEBPB	chr5:178692696-178693007	H1-hESC	embryonic stem cell:	n/a	chr5:178692842-178692853
38	CEBPB	chr5:178705701-178705882	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:178882280-178882457	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr5:178901832-178902147	K562	blood:	n/a	n/a
41	CEBPB	chr5:178820041-178820297	A549	lung:	n/a	n/a
42	CEBPB	chr5:178783581-178783974	IMR90	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
43	CEBPB	chr5:178771987-178772057	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:178819935-178820575	HCT-116	colon:	n/a	n/a
45	CEBPB	chr5:178692543-178693542	IMR90	lung:	n/a	chr5:178692842-178692853
46	CEBPB	chr5:178692615-178693038	HepG2	liver:	n/a	chr5:178692842-178692853
47	CEBPB	chr5:178628252-178628543	Hela-S3	cervix:	n/a	chr5:178628403-178628414
48	CEBPB	chr5:178696901-178697251	IMR90	lung:	n/a	n/a
49	CEBPB	chr5:178820068-178820405	MCF-7	breast:	n/a	n/a
50	CEBPB	chr5:178691969-178692038	HepG2	liver:	n/a	n/a

(count:7331 , 50 per page) page: 1 2 3 4 5 6 7 ... 147

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178833490-178833540	SK-N-SH	brain:	n/a
2	chr5:178854265-178854315	U87	brain:	n/a
3	chr5:178692691-178692741	SK-N-SH_RA	brain:	n/a
4	chr5:178684000-178684050	HNPCEpiC	eye:	n/a
5	chr5:178835980-178836030	GM12878	blood:	n/a
6	chr5:178692806-178692856	K562	blood:	n/a
7	chr5:178772793-178772843	ECC-1	luminal epithelium:	n/a
8	chr5:178774760-178774810	HNPCEpiC	eye:	n/a
9	chr5:178797893-178797943	AG04450	lung:	fetal
10	chr5:178656491-178656541	H1-hESC	embryonic stem cell:	embryo
11	chr5:178770629-178770679	Jurkat	blood:	n/a
12	chr5:178833490-178833540	SK-N-SH	brain:	n/a
13	chr5:178854265-178854315	U87	brain:	n/a
14	chr5:178692691-178692741	SK-N-SH_RA	brain:	n/a
15	chr5:178684000-178684050	HNPCEpiC	eye:	n/a
16	chr5:178835980-178836030	GM12878	blood:	n/a
17	chr5:178692806-178692856	K562	blood:	n/a
18	chr5:178772793-178772843	ECC-1	luminal epithelium:	n/a
19	chr5:178774760-178774810	HNPCEpiC	eye:	n/a
20	chr5:178797893-178797943	AG04450	lung:	fetal
21	chr5:178656491-178656541	H1-hESC	embryonic stem cell:	embryo
22	chr5:178770629-178770679	Jurkat	blood:	n/a
23	chr5:178752999-178753049	BE2_C	brain:	n/a
24	chr5:178704915-178704965	K562	blood:	n/a
25	chr5:178651519-178651569	HUVEC	blood vessel:	n/a
26	chr5:178854586-178854636	AG09309	skin:	n/a
27	chr5:178741004-178741054	IMR90	lung:	fetal
28	chr5:178763771-178763821	AG10803	skin:	n/a
29	chr5:178651200-178651250	HRPEpiC	eye:	n/a
30	chr5:178687780-178687830	GM19239	blood:	n/a
31	chr5:178651519-178651569	MCF10A-Er-Src	breast:	n/a
32	chr5:178835885-178835935	HUVEC	blood vessel:	n/a
33	chr5:178835980-178836030	MCF-7	breast:	n/a
34	chr5:178771781-178771831	PANC-1	pancreas:	n/a
35	chr5:178767472-178767522	NT2-D1	testis:	n/a
36	chr5:178771329-178771379	HepG2	liver:	n/a
37	chr5:178735241-178735291	HAEpiC	amniotic membrane:	n/a
38	chr5:178741004-178741054	HCPEpiC	choroid plexus:	n/a
39	chr5:178667819-178667869	NB4	blood:	n/a
40	chr5:178722726-178722776	AG04449	skin:	fetal
41	chr5:178902790-178902840	HUVEC	blood vessel:	n/a
42	chr5:178684416-178684466	SK-N-MC	brain:	n/a
43	chr5:178651200-178651250	HIPEpiC	eye:	n/a
44	chr5:178799709-178799759	HNPCEpiC	eye:	n/a
45	chr5:178656269-178656319	PrEC	prostate:	n/a
46	chr5:178650512-178650562	A549	lung:	n/a
47	chr5:178654006-178654056	Caco-2	colon:	n/a
48	chr5:178882763-178882813	BJ	skin:	n/a
49	chr5:178800355-178800405	HCF	heart:	n/a
50	chr5:178799709-178799759	HCT-116	colon:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
2	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
3	chr5:178793109..178796105-chr5:179125384..179128079,2	K562	blood:
4	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
5	chr5:178637418..178640045-chr5:178643551..178645345,3	MCF-7	breast:
6	chr5:178649094..178651976-chr5:178660819..178662665,2	MCF-7	breast:
7	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
8	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
9	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
10	chr5:178631257..178632902-chr5:178635722..178638591,2	K562	blood:
11	chr5:178639654..178640533-chr5:178687929..178688900,5	MCF-7	breast:
12	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
13	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
14	chr5:178905653..178907978-chr5:178976399..178978448,2	MCF-7	breast:
15	chr5:178639660..178640480-chr5:178701010..178701947,3	MCF-7	breast:
16	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
17	chr5:178694614..178696834-chr5:178698467..178700770,2	K562	blood:
18	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
19	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
20	chr5:178650614..178652876-chr5:178653305..178655920,2	K562	blood:
21	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
22	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
23	chr5:178669101..178670915-chr5:178673147..178675746,2	MCF-7	breast:
24	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
25	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
26	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
27	chr5:178593807..178594987-chr5:178687910..178688845,5	MCF-7	breast:
28	chr5:178650071..178651966-chr5:178658345..178660809,2	MCF-7	breast:
29	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
30	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
31	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
32	chr5:178698907..178700648-chr5:178703533..178706246,2	MCF-7	breast:
33	chr5:178694647..178697268-chr5:179049140..179050881,2	MCF-7	breast:
34	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
35	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
36	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
37	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
38	chr5:178545417..178547035-chr5:178698975..178701216,2	K562	blood:
39	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
40	chr12:72186780..72187498-chr5:178846162..178846680,2	MCF-7	breast:
41	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
42	chr5:178694614..178696474-chr5:178699270..178701166,2	K562	blood:
43	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
44	chr5:178639654..178640533-chr5:178687929..178688900,5	MCF-7	breast:
45	chr5:178673165..178675582-chr5:178682729..178684288,2	MCF-7	breast:
46	chr5:178626882..178628440-chr5:178635586..178638472,2	MCF-7	breast:
47	chr5:178698907..178700648-chr5:178703533..178706246,2	MCF-7	breast:
48	chr5:178694614..178696474-chr5:178699270..178701166,2	K562	blood:
49	chr5:178673165..178675582-chr5:178682729..178684288,2	MCF-7	breast:
50	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:

(count:10 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 13100 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:13100 , 50 per page) page: 1 2 3 4 5 6 7 ... 262

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552888245	chr5:178627023-178627024	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577511363	chr5:178627056-178627057	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370927541	chr5:178627057-178627058	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79287550	chr5:178627084-178627085	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186241543	chr5:178627183-178627184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368515302	chr5:178627228-178627229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150167890	chr5:178627234-178627235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200419007	chr5:178627240-178627241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562155237	chr5:178627241-178627242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs62397461	chr5:178627244-178627245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75097509	chr5:178627245-178627246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77481814	chr5:178627247-178627248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191786875	chr5:178627289-178627290	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183125629	chr5:178627310-178627311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371861124	chr5:178627311-178627312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567739733	chr5:178627326-178627327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146478157	chr5:178627327-178627328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560119671	chr5:178627336-178627337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533649883	chr5:178627345-178627346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551498614	chr5:178627375-178627376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559709441	chr5:178627410-178627411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528653886	chr5:178627411-178627412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553832376	chr5:178627431-178627432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188159177	chr5:178627448-178627449	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368534551	chr5:178627451-178627452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190848516	chr5:178627457-178627458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182076144	chr5:178627464-178627465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187771365	chr5:178627465-178627466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141305596	chr5:178627470-178627471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571224461	chr5:178627480-178627481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10072825	chr5:178627489-178627490	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556686056	chr5:178627496-178627497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575136714	chr5:178627497-178627498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs535864198	chr5:178627513-178627514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201828209	chr5:178627595-178627596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76630622	chr5:178627619-178627620	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572955906	chr5:178627624-178627625	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536381699	chr5:178627626-178627627	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140561397	chr5:178627656-178627657	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559950607	chr5:178627657-178627658	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143651284	chr5:178627680-178627681	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs3797610	chr5:178627708-178627709	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs549794140	chr5:178627722-178627723	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374794720	chr5:178627767-178627768	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570010870	chr5:178627801-178627802	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530973622	chr5:178627816-178627817	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148176976	chr5:178627837-178627838	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11958443	chr5:178627839-178627840	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528532258	chr5:178627857-178627858	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546412732	chr5:178627866-178627867	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
Thoracic aortic aneurysm	21092924	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3821 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178594800-178627600	Weak transcription	Right Atrium	heart
2	chr5:178607400-178636200	Weak transcription	HSMM	muscle
3	chr5:178607800-178629000	Weak transcription	NHLF	lung
4	chr5:178619000-178635000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:178619600-178627200	Weak transcription	Fetal Intestine Small	intestine
6	chr5:178619800-178650200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr5:178620200-178650200	Weak transcription	Fetal Lung	lung
8	chr5:178620400-178636400	Weak transcription	Ovary	ovary
9	chr5:178621000-178630200	Weak transcription	Osteobl	bone
10	chr5:178622200-178631600	Weak transcription	Spleen	Spleen
11	chr5:178622600-178629200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr5:178622600-178630000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr5:178623200-178629600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:178623800-178628000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:178623800-178633200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:178623800-178636000	Weak transcription	Adipose Nuclei	Adipose
17	chr5:178623800-178636000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr5:178623800-178640600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr5:178624200-178627200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:178624400-178627200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr5:178626400-178628000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:178626600-178629200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:178626600-178629200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:178626600-178630200	Weak transcription	Fetal Stomach	stomach
25	chr5:178626600-178630400	Weak transcription	Esophagus	oesophagus
26	chr5:178626800-178628800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:178626800-178629000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr5:178626800-178629800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:178626800-178636800	Weak transcription	HSMMtube	muscle
30	chr5:178627200-178627600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:178627200-178629600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr5:178627600-178627800	Enhancers	Right Atrium	heart
33	chr5:178627600-178628000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr5:178627600-178628000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr5:178628000-178628400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:178628000-178629200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr5:178628000-178634200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:178628400-178629400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr5:178628800-178630000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:178629000-178629200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:178629000-178630400	Strong transcription	NHLF	lung
42	chr5:178629200-178629800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr5:178629200-178633000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr5:178629200-178635200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:178629200-178636000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr5:178629400-178630600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr5:178629600-178630000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr5:178629600-178630600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr5:178629800-178630200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr5:178629800-178631200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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