Variant report

Variant	nsv883235
Chromosome Location	chr5:178719364-178869884
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1006)
CpG islands
(count:3786)
Chromatin interactive
region (count:44)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1006 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
2	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
4	BACH1	chr5:178753623-178753861	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:178770779-178771405	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:178782018-178782023	K562	blood:	n/a	n/a
7	BACH1	chr5:178867641-178867777	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
9	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
10	BHLHE40	chr5:178722893-178723057	K562	blood:	n/a	chr5:178723031-178723040 chr5:178723031-178723040
11	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
12	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
13	BHLHE40	chr5:178800328-178800428	K562	blood:	n/a	n/a
14	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
15	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
17	CBX3	chr5:178826992-178827587	K562	blood:	n/a	n/a
18	CBX3	chr5:178820032-178820533	HCT-116	colon:	n/a	n/a
19	CBX3	chr5:178827067-178827261	K562	blood:	n/a	n/a
20	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
21	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
22	CEBPB	chr5:178734831-178734994	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:178791997-178792197	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:178858455-178858788	IMR90	lung:	n/a	n/a
25	CEBPB	chr5:178858474-178858798	K562	blood:	n/a	n/a
26	CEBPB	chr5:178858440-178858814	A549	lung:	n/a	n/a
27	CEBPB	chr5:178858441-178858825	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:178780118-178780254	K562	blood:	n/a	n/a
29	CEBPB	chr5:178820068-178820405	MCF-7	breast:	n/a	n/a
30	CEBPB	chr5:178820005-178820443	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:178858362-178858799	MCF-7	breast:	n/a	n/a
32	CEBPB	chr5:178783625-178783949	HepG2	liver:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
33	CEBPB	chr5:178820041-178820297	A549	lung:	n/a	n/a
34	CEBPB	chr5:178731436-178731883	IMR90	lung:	n/a	n/a
35	CEBPB	chr5:178783725-178783925	K562	blood:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
36	CEBPB	chr5:178780036-178780236	IMR90	lung:	n/a	n/a
37	CEBPB	chr5:178786162-178786480	Hela-S3	cervix:	n/a	chr5:178786328-178786339
38	CEBPB	chr5:178858431-178858818	A549	lung:	n/a	n/a
39	CEBPB	chr5:178786289-178786460	HepG2	liver:	n/a	chr5:178786328-178786339
40	CEBPB	chr5:178749384-178749670	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:178786252-178786390	K562	blood:	n/a	chr5:178786328-178786339
42	CEBPB	chr5:178858449-178858788	HepG2	liver:	n/a	n/a
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	chr5:178789476-178789561	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr5:178819993-178820453	IMR90	lung:	n/a	n/a
47	CEBPB	chr5:178783581-178783974	IMR90	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776
48	CEBPB	chr5:178858452-178858788	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr5:178798590-178798744	Hela-S3	cervix:	n/a	chr5:178798651-178798662 chr5:178798649-178798662
50	CEBPB	chr5:178783645-178783928	A549	lung:	n/a	chr5:178783766-178783775 chr5:178783815-178783826 chr5:178783813-178783824 chr5:178783865-178783878 chr5:178783765-178783776

(count:3786 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178741374-178741424	NHDF-neo	bronchial:	n/a
2	chr5:178735241-178735291	HepG2	liver:	n/a
3	chr5:178771329-178771379	RPTEC	kidney:	n/a
4	chr5:178763293-178763343	HRCEpiC	kidney:	n/a
5	chr5:178741374-178741424	NHDF-neo	bronchial:	n/a
6	chr5:178735241-178735291	HepG2	liver:	n/a
7	chr5:178771329-178771379	RPTEC	kidney:	n/a
8	chr5:178763293-178763343	HRCEpiC	kidney:	n/a
9	chr5:178799709-178799759	AG10803	skin:	n/a
10	chr5:178801332-178801382	U87	brain:	n/a
11	chr5:178772203-178772253	Caco-2	colon:	n/a
12	chr5:178752999-178753049	RPTEC	kidney:	n/a
13	chr5:178722726-178722776	HCT-116	colon:	n/a
14	chr5:178775192-178775242	HCM	heart:	n/a
15	chr5:178781563-178781613	SK-N-SH_RA	brain:	n/a
16	chr5:178801647-178801697	BJ	skin:	n/a
17	chr5:178772969-178773019	GM19239	blood:	n/a
18	chr5:178801647-178801697	PFSK-1	brain:	n/a
19	chr5:178808980-178809030	A549	lung:	n/a
20	chr5:178722726-178722776	HCF	heart:	n/a
21	chr5:178753432-178753482	BJ	skin:	n/a
22	chr5:178722726-178722776	HNPCEpiC	eye:	n/a
23	chr5:178741004-178741054	NT2-D1	testis:	n/a
24	chr5:178759017-178759067	Caco-2	colon:	n/a
25	chr5:178753803-178753853	MCF-7	breast:	n/a
26	chr5:178752999-178753049	AG04449	skin:	fetal
27	chr5:178805558-178805608	ovcar-3	ovarian:	n/a
28	chr5:178774760-178774810	Caco-2	colon:	n/a
29	chr5:178763419-178763469	Hepatocyte	liver:	n/a
30	chr5:178767472-178767522	CMK	blood:	n/a
31	chr5:178833490-178833540	HCT-116	colon:	n/a
32	chr5:178854758-178854808	HL-60	blood:	n/a
33	chr5:178772390-178772440	HCM	heart:	n/a
34	chr5:178722726-178722776	K562	blood:	n/a
35	chr5:178752999-178753049	HIPEpiC	eye:	n/a
36	chr5:178797893-178797943	GM19239	blood:	n/a
37	chr5:178772969-178773019	NH-A	brain:	n/a
38	chr5:178854265-178854315	BE2_C	brain:	n/a
39	chr5:178763419-178763469	AG09309	skin:	n/a
40	chr5:178772793-178772843	AG09319	gingival:	n/a
41	chr5:178772793-178772843	SK-N-MC	brain:	n/a
42	chr5:178833490-178833540	GM12891	blood:	n/a
43	chr5:178854586-178854636	AoSMC	blood vessel:	n/a
44	chr5:178801647-178801697	T-47D	breast:	n/a
45	chr5:178741283-178741333	HL-60	blood:	n/a
46	chr5:178772385-178772435	HCT-116	colon:	n/a
47	chr5:178763293-178763343	SK-N-SH_RA	brain:	n/a
48	chr5:178805558-178805608	Caco-2	colon:	n/a
49	chr5:178772969-178773019	AG10803	skin:	n/a
50	chr5:178854502-178854552	HMEC	breast:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:
2	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
3	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
4	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
5	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
6	chr5:178793109..178796105-chr5:179125384..179128079,2	K562	blood:
7	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
8	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
9	chr12:72186780..72187498-chr5:178846162..178846680,2	MCF-7	breast:
10	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
11	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
12	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
13	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
14	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
15	chr5:178815571..178817876-chr5:178818215..178820763,3	MCF-7	breast:
16	chr5:178786828..178788661-chr5:178798258..178800552,2	K562	blood:
17	chr5:178811806..178815884-chr5:178836936..178839970,3	MCF-7	breast:
18	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
19	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
20	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
21	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
22	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
23	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
24	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
25	chr5:178807790..178810700-chr5:178813434..178815392,2	MCF-7	breast:
26	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
27	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
28	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
29	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
30	chr5:178802308..178804471-chr5:178807615..178809965,2	K562	blood:
31	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
32	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
33	chr5:178780858..178782954-chr5:178784606..178786505,2	MCF-7	breast:
34	chr5:178795348..178797290-chr5:178808669..178810729,2	K562	blood:
35	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
36	chr5:178815571..178817876-chr5:178818215..178820763,3	MCF-7	breast:
37	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
38	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
39	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
40	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
41	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
42	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
43	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
44	chr5:178799420..178802506-chr5:178805933..178808859,3	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUFY1-5	chr5:178816913-178817202	l_3076_chr5:178815797-178817202_testes
2	lnc-RUFY1-2	chr5:178805707-178805866	ENSG00000253979
3	lnc-RUFY1-5	chr5:178816320-178816597	l_3076_chr5:178815797-178817202_testes
4	lnc-ADAMTS2-1	chr5:178804601-178804929	XLOC_005105
5	lnc-RUFY1-5	chr5:178815798-178815892	l_3076_chr5:178815797-178817202_testes
6	lnc-ADAMTS2-1	chr5:178805537-178805760	XLOC_005105
7	lnc-RUFY1-2	chr5:178804506-178804705	ENSG00000253979

No data

Variant related genes	Relation type
ADAMTS2	TF binding region
ENSG00000253979	TF binding region
ENSG00000253617	TF binding region
ENSG00000253163	TF binding region
ADAMTS2	CpG island
ENSG00000253979	CpG island
ENSG00000253617	CpG island
ENSG00000253163	CpG island
ENSG00000127022	chromatin interactions
ENSG00000253163	chromatin interactions
ENSG00000253617	chromatin interactions

Extended variants
information (count: 6555 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:6555 , 50 per page) page: 1 2 3 4 5 6 7 ... 132

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4700798	chr5:178719364-178719365	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549412901	chr5:178719415-178719416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192609319	chr5:178719434-178719435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528484550	chr5:178719440-178719441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs163491	chr5:178719448-178719449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372046622	chr5:178719494-178719495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs538782844	chr5:178719555-178719556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551046301	chr5:178719558-178719559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74511260	chr5:178719583-178719584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377145871	chr5:178719599-178719600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1862266	chr5:178719705-178719706	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs554582068	chr5:178719721-178719722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567495293	chr5:178719752-178719753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185575360	chr5:178719796-178719797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536057271	chr5:178719809-178719810	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547300202	chr5:178719816-178719817	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558617841	chr5:178719920-178719921	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576895618	chr5:178719932-178719933	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190053364	chr5:178719944-178719945	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556175435	chr5:178719991-178719992	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575760134	chr5:178720016-178720017	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs163324	chr5:178720043-178720044	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs561270643	chr5:178720125-178720126	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs368161085	chr5:178720142-178720143	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs540509693	chr5:178720151-178720152	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs564979006	chr5:178720152-178720153	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532369043	chr5:178720226-178720227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149669955	chr5:178720250-178720251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145437800	chr5:178720342-178720343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs17079307	chr5:178720394-178720395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181641373	chr5:178720428-178720429	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs539103646	chr5:178720429-178720430	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs184794889	chr5:178720432-178720433	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs534119940	chr5:178720433-178720434	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs188737181	chr5:178720446-178720447	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs116536954	chr5:178720502-178720503	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs535727521	chr5:178720505-178720506	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs148485026	chr5:178720560-178720561	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs556002618	chr5:178720589-178720590	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs3084668	chr5:178720612-178720613	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71869855	chr5:178720613-178720614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs386405808	chr5:178720624-178720625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs57617437	chr5:178720627-178720628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201954494	chr5:178720628-178720629	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs168115	chr5:178720641-178720642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78509577	chr5:178720647-178720648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371489275	chr5:178720654-178720655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554776922	chr5:178720688-178720689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181174668	chr5:178720740-178720741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375755225	chr5:178720764-178720765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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

Chromatin state (count:2047 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178712600-178722200	Weak transcription	Fetal Intestine Small	intestine
2	chr5:178713400-178727200	Weak transcription	NHLF	lung
3	chr5:178714000-178720400	Weak transcription	Fetal Lung	lung
4	chr5:178715000-178720000	Weak transcription	NHDF-Ad	bronchial
5	chr5:178715200-178720000	Weak transcription	Right Atrium	heart
6	chr5:178715200-178722000	Weak transcription	Right Ventricle	heart
7	chr5:178715600-178719800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:178715800-178719800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:178715800-178722400	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr5:178716000-178721400	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr5:178716000-178721400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr5:178716000-178722800	Weak transcription	Spleen	Spleen
13	chr5:178716200-178730800	Weak transcription	HSMM	muscle
14	chr5:178716800-178720000	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr5:178717200-178719800	Weak transcription	HSMMtube	muscle
16	chr5:178717200-178724400	Weak transcription	Ovary	ovary
17	chr5:178718200-178722400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr5:178718200-178725000	Weak transcription	Gastric	stomach
19	chr5:178718400-178719800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:178718400-178720000	Weak transcription	Osteobl	bone
21	chr5:178718400-178720200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr5:178718400-178720600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:178718400-178722800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:178718600-178719800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr5:178718600-178719800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr5:178718800-178719800	Weak transcription	Adipose Nuclei	Adipose
27	chr5:178718800-178721400	Weak transcription	Fetal Stomach	stomach
28	chr5:178719000-178719600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:178719200-178719600	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr5:178719600-178719800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr5:178719600-178721600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr5:178719800-178720000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr5:178719800-178720600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr5:178719800-178720600	Enhancers	Adipose Nuclei	Adipose
35	chr5:178719800-178720600	Enhancers	HSMMtube	muscle
36	chr5:178719800-178720800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr5:178719800-178722400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr5:178719800-178722800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr5:178719800-178725200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr5:178720000-178720200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr5:178720000-178720600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:178720000-178720600	Enhancers	Right Atrium	heart
43	chr5:178720000-178720800	Enhancers	Muscle Satellite Cultured Cells	--
44	chr5:178720000-178722400	Enhancers	NHDF-Ad	bronchial
45	chr5:178720000-178726000	Enhancers	Osteobl	bone
46	chr5:178720200-178720400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr5:178720200-178720800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr5:178720400-178720600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr5:178720400-178720600	Enhancers	Fetal Lung	lung
50	chr5:178720600-178721600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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