Variant report

Variant	nsv1033091
Chromosome Location	chr5:81039194-81159522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3465)
CpG islands
(count:1709)
Chromatin interactive
region (count:181)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3465 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:81054562-81054991	K562	blood:	n/a	n/a
2	ARID3A	chr5:81074562-81075067	K562	blood:	n/a	n/a
3	ARID3A	chr5:81055533-81055748	K562	blood:	n/a	n/a
4	ARID3A	chr5:81049568-81051331	K562	blood:	n/a	n/a
5	ARID3A	chr5:81147301-81148022	K562	blood:	n/a	n/a
6	ARID3A	chr5:81149841-81151200	K562	blood:	n/a	chr5:81150291-81150307 chr5:81150415-81150431
7	ARID3A	chr5:81047152-81047393	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:81059347-81059740	K562	blood:	n/a	n/a
9	ARID3A	chr5:81152725-81153030	K562	blood:	n/a	n/a
10	ARID3A	chr5:81149050-81149611	K562	blood:	n/a	n/a
11	ARID3A	chr5:81048263-81048618	K562	blood:	n/a	n/a
12	ARID3A	chr5:81059998-81060002	K562	blood:	n/a	n/a
13	ARID3A	chr5:81056958-81057213	K562	blood:	n/a	n/a
14	ARID3A	chr5:81057808-81058184	K562	blood:	n/a	n/a
15	ARID3A	chr5:81047100-81047417	K562	blood:	n/a	n/a
16	ARID3A	chr5:81115408-81115443	K562	blood:	n/a	n/a
17	ARID3A	chr5:81134311-81134719	K562	blood:	n/a	n/a
18	ARID3A	chr5:81144264-81144508	K562	blood:	n/a	n/a
19	ATF1	chr5:81046732-81047309	K562	blood:	n/a	n/a
20	ATF1	chr5:81057199-81058024	K562	blood:	n/a	n/a
21	ATF1	chr5:81150785-81150886	K562	blood:	n/a	n/a
22	ATF1	chr5:81147648-81148002	K562	blood:	n/a	n/a
23	ATF1	chr5:81078679-81078991	K562	blood:	n/a	n/a
24	ATF2	chr5:81147632-81148074	GM12878	blood:	n/a	n/a
25	ATF2	chr5:81046629-81047509	GM12878	blood:	n/a	n/a
26	ATF2	chr5:81046961-81047462	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr5:81047037-81047445	GM12878	blood:	n/a	n/a
28	ATF2	chr5:81147234-81148062	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr5:81147528-81148071	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr5:81147543-81148048	GM12878	blood:	n/a	n/a
31	ATF2	chr5:81045141-81045881	GM12878	blood:	n/a	n/a
32	ATF2	chr5:81045187-81045739	GM12878	blood:	n/a	n/a
33	ATF2	chr5:81046902-81047549	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF3	chr5:81147525-81148090	A549	lung:	n/a	n/a
35	ATF3	chr5:81084883-81085140	K562	blood:	n/a	n/a
36	ATF3	chr5:81046976-81047516	A549	lung:	n/a	chr5:81047469-81047478 chr5:81047261-81047270
37	ATF3	chr5:81147585-81147986	A549	lung:	n/a	n/a
38	ATF3	chr5:81069413-81069844	K562	blood:	n/a	n/a
39	ATF3	chr5:81047029-81047461	A549	lung:	n/a	chr5:81047261-81047270
40	ATF3	chr5:81047089-81047411	K562	blood:	n/a	chr5:81047261-81047270
41	BACH1	chr5:81046756-81046995	K562	blood:	n/a	n/a
42	BACH1	chr5:81149975-81150182	K562	blood:	n/a	n/a
43	BACH1	chr5:81047249-81047453	K562	blood:	n/a	n/a
44	BACH1	chr5:81045559-81045802	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr5:81150756-81150977	K562	blood:	n/a	n/a
46	BACH1	chr5:81046703-81047547	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr5:81134387-81134681	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr5:81147611-81148086	H1-hESC	embryonic stem cell:	n/a	n/a
49	BATF	chr5:81147658-81148005	GM12878	blood:	n/a	n/a
50	BATF	chr5:81045329-81045704	GM12878	blood:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:81082946-81082996	AG10803	skin:	n/a
2	chr5:81082946-81082996	AG10803	skin:	n/a
3	chr5:81045966-81046016	HNPCEpiC	eye:	n/a
4	chr5:81075060-81075110	NB4	blood:	n/a
5	chr5:81063103-81063153	GM12892	blood:	n/a
6	chr5:81133592-81133642	K562	blood:	n/a
7	chr5:81047486-81047536	HIPEpiC	eye:	n/a
8	chr5:81048305-81048355	NHBE	bronchial:	n/a
9	chr5:81118892-81118942	ProgFib	skin:	n/a
10	chr5:81147843-81147893	GM19239	blood:	n/a
11	chr5:81146787-81146837	AG04449	skin:	fetal
12	chr5:81045418-81045468	AG04449	skin:	fetal
13	chr5:81048495-81048545	PANC-1	pancreas:	n/a
14	chr5:81152212-81152262	LNCaP	prostate:	n/a
15	chr5:81063103-81063153	NHDF-neo	bronchial:	n/a
16	chr5:81043172-81043222	GM06990	blood:	n/a
17	chr5:81048305-81048355	SK-N-SH	brain:	n/a
18	chr5:81045966-81046016	BJ	skin:	n/a
19	chr5:81075060-81075110	HepG2	liver:	n/a
20	chr5:81047848-81047898	GM12891	blood:	n/a
21	chr5:81047486-81047536	PFSK-1	brain:	n/a
22	chr5:81047184-81047234	GM19239	blood:	n/a
23	chr5:81133592-81133642	NHBE	bronchial:	n/a
24	chr5:81082946-81082996	HIPEpiC	eye:	n/a
25	chr5:81118779-81118829	HCPEpiC	choroid plexus:	n/a
26	chr5:81047249-81047299	SKMC	muscle:	n/a
27	chr5:81118779-81118829	HAEpiC	amniotic membrane:	n/a
28	chr5:81043172-81043222	Hepatocyte	liver:	n/a
29	chr5:81146787-81146837	HUVEC	blood vessel:	n/a
30	chr5:81146787-81146837	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:81084231-81084281	MCF-7	breast:	n/a
32	chr5:81118892-81118942	ovcar-3	ovarian:	n/a
33	chr5:81047848-81047898	AoSMC	blood vessel:	n/a
34	chr5:81144818-81144868	ECC-1	luminal epithelium:	n/a
35	chr5:81147781-81147831	HCM	heart:	n/a
36	chr5:81047184-81047234	NHDF-neo	bronchial:	n/a
37	chr5:81045966-81046016	LNCaP	prostate:	n/a
38	chr5:81047249-81047299	NT2-D1	testis:	n/a
39	chr5:81147781-81147831	HMEC	breast:	n/a
40	chr5:81149002-81149052	HUVEC	blood vessel:	n/a
41	chr5:81084231-81084281	AG09319	gingival:	n/a
42	chr5:81147843-81147893	AG09319	gingival:	n/a
43	chr5:81118892-81118942	HL-60	blood:	n/a
44	chr5:81047184-81047234	NT2-D1	testis:	n/a
45	chr5:81047184-81047234	HRPEpiC	eye:	n/a
46	chr5:81118892-81118942	HNPCEpiC	eye:	n/a
47	chr5:81045418-81045468	SK-N-SH	brain:	n/a
48	chr5:81047486-81047536	SK-N-MC	brain:	n/a
49	chr5:81051199-81051249	MCF-7	breast:	n/a
50	chr5:81045966-81046016	HMEC	breast:	n/a

(count:181 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr5:81045949..81049544-chr5:81078854..81082727,5	MCF-7	breast:
2	chr5:81034741..81036819-chr5:81039221..81041707,2	K562	blood:
3	chr5:81046805..81047696-chr5:81147370..81148097,5	MCF-7	breast:
4	chr5:81146905..81149224-chr5:81149715..81152492,2	MCF-7	breast:
5	chr5:81046445..81049069-chr5:81155209..81157444,2	K562	blood:
6	chr5:81148570..81151043-chr5:81572794..81575109,2	K562	blood:
7	chr5:81069624..81072338-chr5:81075602..81078025,2	K562	blood:
8	chr5:81043503..81052108-chr5:81144332..81149960,26	MCF-7	breast:
9	chr5:81044752..81060050-chr5:81140268..81152732,43	K562	blood:
10	chr5:81121370..81123662-chr5:81126128..81128513,2	K562	blood:
11	chr5:81079948..81083926-chr5:81089732..81092133,3	K562	blood:
12	chr5:81059460..81061720-chr5:81092374..81094863,2	K562	blood:
13	chr5:81046328..81048872-chr5:81065061..81067716,3	MCF-7	breast:
14	chr5:81151621..81154513-chr5:81393425..81396423,2	MCF-7	breast:
15	chr5:81142468..81144614-chr5:81152275..81154478,2	MCF-7	breast:
16	chr5:81042198..81043973-chr5:81054034..81056633,2	K562	blood:
17	chr5:80721034..80721965-chr5:81134326..81134999,2	K562	blood:
18	chr5:81068024..81069829-chr5:81070706..81073662,2	MCF-7	breast:
19	chr5:81147888..81155500-chr5:81156883..81162688,9	K562	blood:
20	chr5:81057535..81060032-chr5:81131821..81133349,2	K562	blood:
21	chr5:81037454..81039351-chr5:81039497..81041595,2	K562	blood:
22	chr5:81108177..81111137-chr5:81117649..81119799,2	K562	blood:
23	chr5:81044026..81052051-chr5:81142054..81153115,35	K562	blood:
24	chr5:81088709..81091547-chr5:81093065..81095903,2	K562	blood:
25	chr5:81083834..81085888-chr5:81131338..81134292,2	K562	blood:
26	chr5:81087373..81090269-chr5:81090799..81094895,4	K562	blood:
27	chr5:81113177..81114943-chr5:81115474..81116978,2	MCF-7	breast:
28	chr5:80959308..80961024-chr5:81090290..81092398,2	K562	blood:
29	chr5:81122190..81125041-chr5:81129394..81132302,2	MCF-7	breast:
30	chr5:81127079..81130458-chr5:81132903..81135987,3	MCF-7	breast:
31	chr5:81046577..81048568-chr5:81151440..81153229,3	MCF-7	breast:
32	chr5:81041105..81043899-chr5:81044992..81047327,2	MCF-7	breast:
33	chr5:81045698..81048740-chr5:81055494..81058903,3	MCF-7	breast:
34	chr5:81047531..81050440-chr5:81268054..81269557,2	K562	blood:
35	chr5:81096228..81099183-chr5:81114424..81117893,3	K562	blood:
36	chr5:81148447..81151496-chr5:81159857..81162688,3	K562	blood:
37	chr5:81147888..81155500-chr5:81156883..81162688,9	K562	blood:
38	chr5:81143314..81145917-chr5:81147794..81150235,3	K562	blood:
39	chr5:81148679..81150688-chr5:81191091..81193118,2	K562	blood:
40	chr5:81077621..81079344-chr5:81094493..81096502,2	K562	blood:
41	chr5:81045699..81050245-chr5:81142897..81150556,22	MCF-7	breast:
42	chr5:81050581..81052753-chr5:81057564..81059448,2	MCF-7	breast:
43	chr5:81102455..81104644-chr5:81115118..81117912,2	K562	blood:
44	chr5:81147694..81150688-chr5:81266615..81269918,3	K562	blood:
45	chr5:81102455..81104644-chr5:81115118..81117912,2	K562	blood:
46	chr5:81046777..81047952-chr5:81146745..81148237,8	MCF-7	breast:
47	chr5:81045915..81048135-chr5:81141025..81142664,2	MCF-7	breast:
48	chr5:81059460..81061720-chr5:81092374..81094863,2	K562	blood:
49	chr5:81113177..81114943-chr5:81115474..81116978,2	MCF-7	breast:
50	chr5:81046741..81048701-chr5:81134224..81135770,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATG10-3	chr5:81147420-81148020	ENSG00000249483

No data

Variant related genes	Relation type
ENSG00000249483	TF binding region
SSBP2	TF binding region
ENSG00000249483	CpG island
SSBP2	CpG island
ENSG00000186468	chromatin interactions
ENSG00000249483	chromatin interactions
ENSG00000145687	chromatin interactions
ENSG00000152348	chromatin interactions

Extended variants
information (count: 3809 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3809 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369618585	chr5:81039198-81039199	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs535223259	chr5:81039237-81039238	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs546888226	chr5:81039249-81039250	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545021420	chr5:81039274-81039275	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146614748	chr5:81039322-81039323	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140974176	chr5:81039353-81039354	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575615634	chr5:81039359-81039360	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536675019	chr5:81039360-81039361	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs10213685	chr5:81039377-81039378	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs576567625	chr5:81039447-81039448	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs35880021	chr5:81039463-81039464	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs371376021	chr5:81039500-81039501	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs185016579	chr5:81039508-81039509	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs369012854	chr5:81039517-81039518	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552892587	chr5:81039525-81039526	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574644757	chr5:81039575-81039576	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541744519	chr5:81039647-81039648	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376140071	chr5:81039671-81039672	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150222589	chr5:81039711-81039712	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530926075	chr5:81039775-81039776	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs34007998	chr5:81039817-81039818	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs536123706	chr5:81039967-81039968	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9688025	chr5:81040002-81040003	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs188259382	chr5:81040024-81040025	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114834986	chr5:81040055-81040056	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs568576733	chr5:81040114-81040115	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145684555	chr5:81040151-81040152	Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs74465471	chr5:81040205-81040206	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181860335	chr5:81040223-81040224	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148928869	chr5:81040230-81040231	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs58821505	chr5:81040253-81040254	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187018660	chr5:81040289-81040290	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570163317	chr5:81040295-81040296	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs1550803	chr5:81040312-81040313	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs192309615	chr5:81040351-81040352	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs566128923	chr5:81040352-81040353	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553069491	chr5:81040363-81040364	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147047597	chr5:81040377-81040378	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs1550804	chr5:81040392-81040393	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562652038	chr5:81040430-81040431	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373621892	chr5:81040431-81040432	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs13160079	chr5:81040441-81040442	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs561375202	chr5:81040457-81040458	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183320904	chr5:81040483-81040484	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546174062	chr5:81040561-81040562	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs115119216	chr5:81040574-81040575	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs138192664	chr5:81040720-81040721	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187032120	chr5:81040792-81040793	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540354506	chr5:81040798-81040799	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562238268	chr5:81040814-81040815	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Tetralogy of Fallot	22912587	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3359 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:81008800-81044800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:81016000-81044800	Weak transcription	Fetal Stomach	stomach
3	chr5:81020800-81039200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr5:81028600-81044200	Weak transcription	Primary B cells from cord blood	blood
5	chr5:81029800-81040800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:81030200-81043000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:81030400-81039600	Weak transcription	Primary T cells from cord blood	blood
8	chr5:81031800-81040400	Weak transcription	Fetal Brain Female	brain
9	chr5:81031800-81043000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr5:81032000-81045000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr5:81032200-81043600	Weak transcription	Fetal Lung	lung
12	chr5:81032200-81044400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr5:81032200-81045000	Weak transcription	Ovary	ovary
14	chr5:81032200-81045000	Weak transcription	Psoas Muscle	Psoas
15	chr5:81032200-81045200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:81032200-81045200	Weak transcription	Esophagus	oesophagus
17	chr5:81032200-81045200	Weak transcription	Pancreas	Pancrea
18	chr5:81032600-81044800	Weak transcription	HSMM	muscle
19	chr5:81033800-81042000	Genic enhancers	Dnd41	blood
20	chr5:81034000-81042200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr5:81034600-81041800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr5:81035000-81044200	Weak transcription	Thymus	Thymus
23	chr5:81035400-81041800	Weak transcription	Primary hematopoietic stem cells	blood
24	chr5:81035400-81045000	Weak transcription	Left Ventricle	heart
25	chr5:81035600-81044600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:81036400-81040000	Strong transcription	Fetal Thymus	thymus
27	chr5:81036400-81042800	Weak transcription	NHLF	lung
28	chr5:81036600-81040200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr5:81036600-81044200	Weak transcription	Fetal Heart	heart
30	chr5:81036800-81039600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr5:81036800-81040400	Weak transcription	Brain Germinal Matrix	brain
32	chr5:81036800-81044600	Weak transcription	Fetal Kidney	kidney
33	chr5:81037000-81041600	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr5:81037000-81043000	Weak transcription	Colon Smooth Muscle	Colon
35	chr5:81037200-81042000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr5:81037200-81045000	Weak transcription	Fetal Muscle Leg	muscle
37	chr5:81037600-81039200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:81037600-81044400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr5:81038200-81040000	Enhancers	Fetal Brain Male	brain
40	chr5:81038400-81039800	ZNF genes & repeats	GM12878-XiMat	blood
41	chr5:81038600-81039600	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr5:81038600-81040000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr5:81038600-81040200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:81038600-81044400	Weak transcription	K562	blood
45	chr5:81038600-81045200	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr5:81038800-81042200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr5:81039000-81039400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr5:81039200-81039600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:81039200-81039800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr5:81039400-81039600	Weak transcription	Brain Angular Gyrus	brain

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