Variant report

Variant	nsv882362
Chromosome Location	chr5:89437963-89604380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1177)
CpG islands
(count:367)
Chromatin interactive
region (count:55)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1177 , 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	ATF1	chr5:89589858-89590065	K562	blood:	n/a	n/a
2	ATF2	chr5:89560911-89561458	GM12878	blood:	n/a	n/a
3	BCLAF1	chr5:89561038-89561409	GM12878	blood:	n/a	n/a
4	BCLAF1	chr5:89560852-89561423	GM12878	blood:	n/a	n/a
5	BHLHE40	chr5:89563533-89563749	K562	blood:	n/a	chr5:89563661-89563670 chr5:89563660-89563669 chr5:89563661-89563670
6	BHLHE40	chr5:89561084-89561386	GM12878	blood:	n/a	n/a
7	BHLHE40	chr5:89561861-89561975	GM12878	blood:	n/a	n/a
8	BRCA1	chr5:89601037-89601096	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr5:89593250-89593363	K562	blood:	n/a	n/a
10	CEBPB	chr5:89478490-89479052	MCF-7	breast:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
11	CEBPB	chr5:89480125-89480178	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr5:89603380-89603850	MCF-7	breast:	n/a	n/a
13	CEBPB	chr5:89553910-89553997	K562	blood:	n/a	chr5:89553938-89553949
14	CEBPB	chr5:89517620-89518194	MCF-7	breast:	n/a	n/a
15	CEBPB	chr5:89558712-89558951	A549	lung:	n/a	chr5:89558802-89558815 chr5:89558802-89558813 chr5:89558804-89558815 chr5:89558842-89558853
16	CEBPB	chr5:89558671-89558964	HepG2	liver:	n/a	chr5:89558802-89558815 chr5:89558802-89558813 chr5:89558804-89558815 chr5:89558842-89558853
17	CEBPB	chr5:89479145-89479330	K562	blood:	n/a	n/a
18	CEBPB	chr5:89553804-89554111	HepG2	liver:	n/a	chr5:89553938-89553949
19	CEBPB	chr5:89478585-89478897	Hela-S3	cervix:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
20	CEBPB	chr5:89479193-89479407	HepG2	liver:	n/a	chr5:89479325-89479336
21	CEBPB	chr5:89478395-89479106	MCF-7	breast:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
22	CEBPB	chr5:89478743-89478746	K562	blood:	n/a	n/a
23	CEBPB	chr5:89478598-89478876	HepG2	liver:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
24	CEBPB	chr5:89561013-89561318	MCF-7	breast:	n/a	n/a
25	CEBPB	chr5:89590722-89590799	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr5:89478677-89478896	A549	lung:	n/a	chr5:89478732-89478745 chr5:89478734-89478745 chr5:89478732-89478743
27	CEBPB	chr5:89561095-89561384	K562	blood:	n/a	n/a
28	CEBPB	chr5:89558647-89558962	IMR90	lung:	n/a	chr5:89558802-89558815 chr5:89558802-89558813 chr5:89558804-89558815 chr5:89558842-89558853
29	CEBPB	chr5:89497745-89498184	HCT-116	colon:	n/a	n/a
30	CHD1	chr5:89590793-89590812	GM12878	blood:	n/a	n/a
31	CHD1	chr5:89504051-89504058	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:89561220-89561370	NHDF-neo	bronchial:	n/a	chr5:89561272-89561290 chr5:89561267-89561288 chr5:89561273-89561289 chr5:89561274-89561287
33	CTCF	chr5:89590540-89590690	GM12872	blood:	n/a	n/a
34	CTCF	chr5:89481200-89481350	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr5:89600520-89600670	HPAF	blood vessel:	n/a	chr5:89600590-89600608
36	CTCF	chr5:89457320-89457470	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr5:89457400-89457550	HPAF	blood vessel:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
38	CTCF	chr5:89590520-89590670	SAEC	small airway:	n/a	n/a
39	CTCF	chr5:89593304-89593392	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:89561180-89561330	HRE	kidney:	n/a	chr5:89561272-89561290 chr5:89561267-89561288 chr5:89561273-89561289 chr5:89561274-89561287
41	CTCF	chr5:89460011-89460178	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:89460000-89460150	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr5:89457380-89457530	HepG2	liver:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
44	CTCF	chr5:89590513-89590677	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:89481220-89481370	HPF	lung:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
46	CTCF	chr5:89481280-89481430	RPTEC	kidney:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
47	CTCF	chr5:89561105-89561391	HepG2	liver:	n/a	chr5:89561272-89561290 chr5:89561267-89561288 chr5:89561273-89561289 chr5:89561274-89561287
48	CTCF	chr5:89457400-89457550	NHDF-neo	bronchial:	n/a	chr5:89457504-89457522 chr5:89457506-89457519 chr5:89457499-89457520
49	CTCF	chr5:89481220-89481370	HA-sp	spinal cord:	n/a	chr5:89481339-89481357 chr5:89481334-89481355 chr5:89481340-89481356
50	CTCF	chr5:89590480-89590630	HRE	kidney:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:89504421-89504471	PFSK-1	brain:	n/a
2	chr5:89504421-89504471	PFSK-1	brain:	n/a
3	chr5:89560863-89560913	AG04450	lung:	fetal
4	chr5:89549625-89549675	HAEpiC	amniotic membrane:	n/a
5	chr5:89560863-89560913	HEK293	kidney:	embryo
6	chr5:89560863-89560913	HL-60	blood:	n/a
7	chr5:89560863-89560913	HPAEpiC	pulmonary alveolar:	n/a
8	chr5:89504421-89504471	SKMC	muscle:	n/a
9	chr5:89549625-89549675	T-47D	breast:	n/a
10	chr5:89549625-89549675	NT2-D1	testis:	n/a
11	chr5:89593497-89593547	NHDF-neo	bronchial:	n/a
12	chr5:89593497-89593547	Hepatocyte	liver:	n/a
13	chr5:89600962-89601012	HepG2	liver:	n/a
14	chr5:89600962-89601012	PrEC	prostate:	n/a
15	chr5:89600962-89601012	U87	brain:	n/a
16	chr5:89549625-89549675	GM06990	blood:	n/a
17	chr5:89549625-89549675	IMR90	lung:	fetal
18	chr5:89593497-89593547	HAEpiC	amniotic membrane:	n/a
19	chr5:89549625-89549675	CMK	blood:	n/a
20	chr5:89504421-89504471	K562	blood:	n/a
21	chr5:89504421-89504471	AoSMC	blood vessel:	n/a
22	chr5:89504421-89504471	NHBE	bronchial:	n/a
23	chr5:89600962-89601012	SK-N-SH_RA	brain:	n/a
24	chr5:89504421-89504471	BJ	skin:	n/a
25	chr5:89549625-89549675	GM12892	blood:	n/a
26	chr5:89593497-89593547	HCPEpiC	choroid plexus:	n/a
27	chr5:89504421-89504471	U87	brain:	n/a
28	chr5:89549625-89549675	HepG2	liver:	n/a
29	chr5:89593497-89593547	AG10803	skin:	n/a
30	chr5:89600962-89601012	NT2-D1	testis:	n/a
31	chr5:89560863-89560913	ProgFib	skin:	n/a
32	chr5:89600962-89601012	Hela-S3	cervix:	n/a
33	chr5:89458394-89458444	BJ	skin:	n/a
34	chr5:89549625-89549675	HUVEC	blood vessel:	n/a
35	chr5:89504421-89504471	HEEpiC	esophagus:	n/a
36	chr5:89560863-89560913	T-47D	breast:	n/a
37	chr5:89549625-89549675	ProgFib	skin:	n/a
38	chr5:89504421-89504471	H1-hESC	embryonic stem cell:	embryo
39	chr5:89593497-89593547	NH-A	brain:	n/a
40	chr5:89458394-89458444	HRCEpiC	kidney:	n/a
41	chr5:89593497-89593547	AG04450	lung:	fetal
42	chr5:89549625-89549675	Hepatocyte	liver:	n/a
43	chr5:89560863-89560913	AG09309	skin:	n/a
44	chr5:89458394-89458444	BE2_C	brain:	n/a
45	chr5:89504421-89504471	ovcar-3	ovarian:	n/a
46	chr5:89549625-89549675	HCF	heart:	n/a
47	chr5:89600962-89601012	BE2_C	brain:	n/a
48	chr5:89549625-89549675	HCM	heart:	n/a
49	chr5:89600962-89601012	HRE	kidney:	n/a
50	chr5:89600962-89601012	NB4	blood:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:89600856..89602668-chr5:89604129..89605758,2	MCF-7	breast:
2	chr5:88025172..88025905-chr5:89457296..89457865,2	MCF-7	breast:
3	chr5:89548610..89551361-chr5:89563315..89565634,2	K562	blood:
4	chr5:89478001..89478682-chr5:89560766..89561737,2	MCF-7	breast:
5	chr5:89575312..89576914-chr5:89580141..89581682,2	K562	blood:
6	chr5:89564889..89568033-chr5:89575518..89579089,3	MCF-7	breast:
7	chr19:47452350..47452852-chr5:89481098..89481635,2	MCF-7	breast:
8	chr5:89591158..89592790-chr5:89596233..89598703,2	K562	blood:
9	chr5:88023266..88024159-chr5:89481181..89482220,3	MCF-7	breast:
10	chr5:89440122..89441898-chr5:89710102..89712875,2	K562	blood:
11	chr5:89450263..89452091-chr5:89459803..89462765,2	K562	blood:
12	chr5:89464195..89466496-chr5:89478759..89480447,2	MCF-7	breast:
13	chr5:89574997..89576812-chr5:89578806..89581682,2	K562	blood:
14	chr1:200638121..200638819-chr5:89558663..89559163,2	Hela-S3	cervix:
15	chr5:89600856..89602668-chr5:89604129..89605758,2	MCF-7	breast:
16	chr5:89552564..89556289-chr5:89558492..89560560,3	K562	blood:
17	chr5:89587624..89591345-chr5:89704082..89707436,4	MCF-7	breast:
18	chr5:89518716..89521688-chr5:89521836..89523826,2	K562	blood:
19	chr5:89492241..89495150-chr5:89499571..89502456,2	MCF-7	breast:
20	chr5:89550009..89551577-chr5:89552431..89555407,2	K562	blood:
21	chr5:89590585..89592535-chr5:89603393..89605933,2	K562	blood:
22	chr5:89492241..89495150-chr5:89499571..89502456,2	MCF-7	breast:
23	chr5:89577446..89579858-chr5:89581401..89583699,2	K562	blood:
24	chr5:89486075..89488645-chr5:89498532..89500910,2	MCF-7	breast:
25	chr5:89567192..89569366-chr5:89570878..89572934,2	K562	blood:
26	chr5:89518716..89521688-chr5:89521836..89523826,2	K562	blood:
27	chr5:89488777..89489596-chr5:89560837..89561562,2	MCF-7	breast:
28	chr5:89574997..89576812-chr5:89578806..89581682,2	K562	blood:
29	chr5:89540752..89543212-chr5:89703513..89705580,2	K562	blood:
30	chr5:89431785..89432445-chr5:89480883..89481450,2	MCF-7	breast:
31	chr5:89550009..89551577-chr5:89552431..89555407,2	K562	blood:
32	chr5:89577446..89579858-chr5:89581401..89583699,2	K562	blood:
33	chr5:89424577..89427181-chr5:89477384..89480232,2	MCF-7	breast:
34	chr5:89478001..89478682-chr5:89560766..89561737,2	MCF-7	breast:
35	chr5:89548610..89551361-chr5:89563315..89565634,2	K562	blood:
36	chr5:89485697..89486219-chr6:16818547..16819067,2	MCF-7	breast:
37	chr5:88023665..88024220-chr5:89560775..89561684,4	MCF-7	breast:
38	chr5:89478032..89480920-chr5:89706398..89708148,2	K562	blood:
39	chr5:89552564..89556289-chr5:89558492..89560560,3	K562	blood:
40	chr5:89567192..89569366-chr5:89570878..89572934,2	K562	blood:
41	chr5:89486075..89488645-chr5:89498532..89500910,2	MCF-7	breast:
42	chr5:89464195..89466496-chr5:89478759..89480447,2	MCF-7	breast:
43	chr5:89564889..89568033-chr5:89575518..89579089,3	MCF-7	breast:
44	chr5:89450263..89452091-chr5:89459803..89462765,2	K562	blood:
45	chr5:89431375..89432368-chr5:89560789..89562074,8	MCF-7	breast:
46	chr5:89603872..89605445-chr5:89703520..89706240,2	MCF-7	breast:
47	chr5:89431318..89432484-chr5:89560747..89561819,9	MCF-7	breast:
48	chr5:89488777..89489596-chr5:89560837..89561562,2	MCF-7	breast:
49	chr5:89225139..89225642-chr5:89457055..89457700,2	MCF-7	breast:
50	chr5:89575312..89576914-chr5:89580141..89581682,2	K562	blood:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CETN3-3	chr5:89556363-89556403	ENSG00000248555
2	lnc-CETN3-3	chr5:89585713-89585888	ENSG00000248555
3	lnc-CETN3-4	chr5:89567005-89567108	l_2968_chr5:89567004-89621626_testes
4	lnc-CETN3-3	chr5:89454173-89454336	ENSG00000248555
5	lnc-CETN3-3	chr5:89530743-89530782	ENSG00000248555
6	lnc-CETN3-3	chr5:89455806-89455940	ENSG00000248555
7	lnc-CETN3-4	chr5:89592119-89592149	l_2968_chr5:89567004-89621626_testes
8	lnc-CETN3-3	chr5:89496284-89496345	ENSG00000248555
9	lnc-CETN3-3	chr5:89557485-89557536	ENSG00000248555
10	lnc-CETN3-3	chr5:89556363-89556403	ENSG00000248555
11	lnc-CETN3-3	chr5:89456346-89456450	ENSG00000248555
12	lnc-CETN3-3	chr5:89585713-89585798	ENSG00000248555
13	lnc-CETN3-3	chr5:89585713-89585755	ENSG00000248555
14	lnc-CETN3-3	chr5:89456346-89456406	ENSG00000248555
15	lnc-CETN3-3	chr5:89556363-89556403	ENSG00000248555
16	lnc-CETN3-4	chr5:89593245-89593292	l_2968_chr5:89567004-89621626_testes
17	lnc-CETN3-3	chr5:89456346-89456406	ENSG00000248555
18	lnc-CETN3-5	chr5:89575332-89575353	NONHSAT102725
19	lnc-CETN3-5	chr5:89561079-89561383	NONHSAT102725
20	lnc-CETN3-3	chr5:89531246-89531352	ENSG00000248555
21	lnc-CETN3-3	chr5:89454156-89454336	ENSG00000248555
22	lnc-CETN3-4	chr5:89596768-89597139	l_2968_chr5:89567004-89621626_testes
23	lnc-CETN3-3	chr5:89557485-89557536	ENSG00000248555
24	lnc-CETN3-3	chr5:89540428-89540572	ENSG00000248555
25	lnc-CETN3-3	chr5:89557485-89557536	ENSG00000248555

No data

Variant related genes	Relation type
ENSG00000248555	TF binding region
ENSG00000248555	CpG island
ENSG00000153140	chromatin interactions
ENSG00000255647	chromatin interactions
ENSG00000260088	chromatin interactions
ENSG00000081189	chromatin interactions

Extended variants
information (count: 5111 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5111 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2366398	chr5:89437963-89437964	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189155313	chr5:89437982-89437983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376335722	chr5:89437986-89437987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75384908	chr5:89438036-89438037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180997978	chr5:89438046-89438047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186194874	chr5:89438054-89438055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572788300	chr5:89438081-89438082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150012450	chr5:89438107-89438108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs533078755	chr5:89438108-89438109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546535191	chr5:89438140-89438141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189435357	chr5:89438146-89438147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368584030	chr5:89438172-89438173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528109247	chr5:89438182-89438183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529084378	chr5:89438190-89438191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181442143	chr5:89438213-89438214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145313549	chr5:89438241-89438242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79257261	chr5:89438296-89438297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538302699	chr5:89438362-89438363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558526754	chr5:89438478-89438479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557879039	chr5:89438518-89438519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375349636	chr5:89438551-89438552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145151753	chr5:89438561-89438562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146889345	chr5:89438577-89438578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373047690	chr5:89438587-89438588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574372654	chr5:89438610-89438611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543265360	chr5:89438644-89438645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186821140	chr5:89438650-89438651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575252297	chr5:89438703-89438704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs544247346	chr5:89438755-89438756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140794223	chr5:89438822-89438823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144628846	chr5:89438860-89438861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191267526	chr5:89438872-89438873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148193987	chr5:89438935-89438936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141181077	chr5:89438939-89438940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544534461	chr5:89438984-89438985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183021288	chr5:89438985-89438986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2950032	chr5:89438995-89438996	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs150327455	chr5:89439007-89439008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs367573208	chr5:89439017-89439018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374090582	chr5:89439031-89439032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138018770	chr5:89439047-89439048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114481609	chr5:89439080-89439081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6898716	chr5:89439105-89439106	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs186760113	chr5:89439113-89439114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143657928	chr5:89439159-89439160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2920514	chr5:89439228-89439229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556482080	chr5:89439335-89439336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369682088	chr5:89439459-89439460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147214645	chr5:89439520-89439521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140658684	chr5:89439534-89439535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	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
Esophageal adenocarcinoma	18519675	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
Ovarian cancer	21720365	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
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:89432200-89442600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:89432200-89442600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:89437800-89439000	Enhancers	Primary B cells from peripheral blood	blood
4	chr5:89438000-89438600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:89438000-89439000	Enhancers	Primary B cells from cord blood	blood
6	chr5:89438400-89438600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:89438600-89438800	Enhancers	Placenta Amnion	Placenta Amnion
8	chr5:89438600-89439800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr5:89438600-89441400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:89439000-89440200	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr5:89439600-89440600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr5:89439600-89441000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:89439800-89440800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr5:89440000-89440200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr5:89440000-89441600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:89440200-89440400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr5:89440200-89440600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr5:89440200-89441000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:89440200-89441000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr5:89440200-89441000	Enhancers	Placenta Amnion	Placenta Amnion
21	chr5:89440200-89441000	Enhancers	HUVEC	blood vessel
22	chr5:89440200-89441200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr5:89440400-89441000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr5:89440600-89442600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr5:89442200-89442800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
26	chr5:89442600-89443400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr5:89442600-89443400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:89443400-89457000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:89449000-89449600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr5:89449200-89449600	Active TSS	Spleen	Spleen
31	chr5:89452000-89452200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:89452200-89454200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:89452800-89454400	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr5:89453200-89454000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr5:89453800-89454400	Enhancers	Colon Smooth Muscle	Colon
36	chr5:89454000-89454400	Enhancers	GM12878-XiMat	blood
37	chr5:89454200-89454400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:89454200-89454800	Enhancers	Ovary	ovary
39	chr5:89454200-89454800	Enhancers	HSMMtube	muscle
40	chr5:89454800-89456800	Weak transcription	Ovary	ovary
41	chr5:89456400-89457200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:89456800-89457600	Enhancers	Ovary	ovary
43	chr5:89456800-89457600	Enhancers	Stomach Mucosa	stomach
44	chr5:89457000-89457200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:89457000-89457600	Enhancers	Pancreas	Pancrea
46	chr5:89457000-89457600	Enhancers	Right Atrium	heart
47	chr5:89457000-89457600	Enhancers	Spleen	Spleen
48	chr5:89457200-89457400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:89457200-89457600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:89457200-89457600	Enhancers	Adipose Nuclei	Adipose

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