Variant report

Variant	esv1803747
Chromosome Location	chr3:93602038-93759079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1509)
CpG islands
(count:1894)
Chromatin interactive
region (count:81)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1509 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:93690348-93690789	K562	blood:	n/a	n/a
2	ARID3A	chr3:93698649-93699202	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:93691767-93692970	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:93692592-93692986	K562	blood:	n/a	n/a
5	ARID3A	chr3:93676282-93676501	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:93642022-93642172	K562	blood:	n/a	n/a
7	ATF1	chr3:93688928-93689209	K562	blood:	n/a	n/a
8	ATF1	chr3:93692661-93693084	K562	blood:	n/a	n/a
9	ATF1	chr3:93698620-93699143	K562	blood:	n/a	n/a
10	ATF3	chr3:93688877-93689155	K562	blood:	n/a	n/a
11	ATF3	chr3:93698831-93699098	K562	blood:	n/a	chr3:93698974-93698987
12	BACH1	chr3:93692288-93692715	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:93713979-93714016	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr3:93655969-93656191	GM12878	blood:	n/a	n/a
15	BCLAF1	chr3:93698872-93699504	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:93688299-93688633	K562	blood:	n/a	n/a
17	BHLHE40	chr3:93690516-93690676	K562	blood:	n/a	n/a
18	BHLHE40	chr3:93698432-93699352	K562	blood:	n/a	n/a
19	BHLHE40	chr3:93698741-93699514	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:93692454-93693052	K562	blood:	n/a	n/a
21	BRCA1	chr3:93692300-93692913	HepG2	liver:	n/a	n/a
22	BRCA1	chr3:93698708-93699567	Hela-S3	cervix:	n/a	chr3:93699508-93699515
23	BRCA1	chr3:93698957-93699082	HepG2	liver:	n/a	n/a
24	CBX3	chr3:93661017-93661284	K562	blood:	n/a	n/a
25	CBX3	chr3:93660944-93661275	K562	blood:	n/a	n/a
26	CBX3	chr3:93625948-93626194	K562	blood:	n/a	n/a
27	CBX3	chr3:93700392-93700721	K562	blood:	n/a	n/a
28	CBX3	chr3:93692607-93693038	K562	blood:	n/a	n/a
29	CCNT2	chr3:93698783-93699452	K562	blood:	n/a	n/a
30	CCNT2	chr3:93688880-93689213	K562	blood:	n/a	n/a
31	CCNT2	chr3:93692423-93693063	K562	blood:	n/a	chr3:93692940-93692949
32	CEBPB	chr3:93693229-93693381	K562	blood:	n/a	n/a
33	CEBPB	chr3:93683888-93684166	A549	lung:	n/a	chr3:93684037-93684048
34	CEBPB	chr3:93692007-93692174	HepG2	liver:	n/a	n/a
35	CEBPB	chr3:93690689-93691261	K562	blood:	n/a	chr3:93690752-93690765 chr3:93690752-93690765 chr3:93691136-93691147 chr3:93691136-93691147
36	CEBPB	chr3:93736618-93736843	K562	blood:	n/a	chr3:93736693-93736704
37	CEBPB	chr3:93629053-93629308	K562	blood:	n/a	chr3:93629160-93629171 chr3:93629159-93629172 chr3:93629159-93629170
38	CEBPB	chr3:93688933-93689299	K562	blood:	n/a	n/a
39	CEBPB	chr3:93691906-93692431	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:93650513-93650709	HepG2	liver:	n/a	chr3:93650686-93650699 chr3:93650686-93650697
41	CEBPB	chr3:93615540-93615692	K562	blood:	n/a	chr3:93615585-93615598
42	CEBPB	chr3:93691900-93692927	HepG2	liver:	n/a	n/a
43	CEBPB	chr3:93700376-93700715	K562	blood:	n/a	n/a
44	CEBPB	chr3:93650673-93650708	K562	blood:	n/a	chr3:93650686-93650699 chr3:93650686-93650697
45	CEBPB	chr3:93683932-93684221	HepG2	liver:	n/a	chr3:93684037-93684048
46	CEBPB	chr3:93698943-93699110	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:93628924-93629461	Hela-S3	cervix:	n/a	chr3:93629160-93629171 chr3:93628939-93628950 chr3:93629159-93629172 chr3:93629159-93629170
48	CEBPB	chr3:93704056-93704242	K562	blood:	n/a	chr3:93704193-93704206
49	CEBPB	chr3:93716756-93716887	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr3:93649629-93649633	K562	blood:	n/a	n/a

(count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:93689422-93689472	HNPCEpiC	eye:	n/a
2	chr3:93747410-93747460	HPAEpiC	pulmonary alveolar:	n/a
3	chr3:93693147-93693197	HCF	heart:	n/a
4	chr3:93689422-93689472	HNPCEpiC	eye:	n/a
5	chr3:93747410-93747460	HPAEpiC	pulmonary alveolar:	n/a
6	chr3:93693147-93693197	HCF	heart:	n/a
7	chr3:93747528-93747578	GM12878	blood:	n/a
8	chr3:93692952-93693002	SK-N-MC	brain:	n/a
9	chr3:93698964-93699014	Hela-S3	cervix:	n/a
10	chr3:93698964-93699014	LNCaP	prostate:	n/a
11	chr3:93692925-93692975	ProgFib	skin:	n/a
12	chr3:93698461-93698511	ProgFib	skin:	n/a
13	chr3:93740824-93740874	SK-N-MC	brain:	n/a
14	chr3:93747528-93747578	ProgFib	skin:	n/a
15	chr3:93698928-93698978	GM12891	blood:	n/a
16	chr3:93699019-93699069	NT2-D1	testis:	n/a
17	chr3:93647007-93647057	HNPCEpiC	eye:	n/a
18	chr3:93702658-93702708	MCF-7	breast:	n/a
19	chr3:93698964-93699014	HCM	heart:	n/a
20	chr3:93698231-93698281	K562	blood:	n/a
21	chr3:93747410-93747460	HepG2	liver:	n/a
22	chr3:93740824-93740874	HRCEpiC	kidney:	n/a
23	chr3:93698533-93698583	Caco-2	colon:	n/a
24	chr3:93702658-93702708	GM19239	blood:	n/a
25	chr3:93698461-93698511	HCM	heart:	n/a
26	chr3:93698939-93698989	HIPEpiC	eye:	n/a
27	chr3:93692764-93692814	MCF-7	breast:	n/a
28	chr3:93698461-93698511	MCF-7	breast:	n/a
29	chr3:93694020-93694070	HRE	kidney:	n/a
30	chr3:93677738-93677788	Hepatocyte	liver:	n/a
31	chr3:93696108-93696158	AG10803	skin:	n/a
32	chr3:93692773-93692823	HEK293	kidney:	embryo
33	chr3:93647605-93647655	NHDF-neo	bronchial:	n/a
34	chr3:93692564-93692614	IMR90	lung:	fetal
35	chr3:93677738-93677788	AG09319	gingival:	n/a
36	chr3:93646378-93646428	NH-A	brain:	n/a
37	chr3:93699019-93699069	SK-N-MC	brain:	n/a
38	chr3:93692773-93692823	Hepatocyte	liver:	n/a
39	chr3:93698461-93698511	GM12892	blood:	n/a
40	chr3:93698533-93698583	GM19239	blood:	n/a
41	chr3:93733689-93733739	SK-N-SH	brain:	n/a
42	chr3:93747410-93747460	NT2-D1	testis:	n/a
43	chr3:93693147-93693197	GM12878	blood:	n/a
44	chr3:93699352-93699402	Hela-S3	cervix:	n/a
45	chr3:93698533-93698583	AoSMC	blood vessel:	n/a
46	chr3:93698461-93698511	CMK	blood:	n/a
47	chr3:93677738-93677788	HUVEC	blood vessel:	n/a
48	chr3:93698461-93698511	SKMC	muscle:	n/a
49	chr3:93696108-93696158	GM12878	blood:	n/a
50	chr3:93698768-93698818	Jurkat	blood:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:93679066..93681793-chr3:93685442..93688192,2	K562	blood:
2	chr3:93734850..93736362-chr3:93780454..93782213,2	MCF-7	breast:
3	chr3:93690925..93693157-chr3:93696535..93699093,2	MCF-7	breast:
4	chr3:93654201..93655762-chr3:93660898..93663750,2	MCF-7	breast:
5	chr3:93700627..93702647-chr3:93720581..93722935,2	MCF-7	breast:
6	chr3:93722234..93724634-chr3:93733108..93735943,2	K562	blood:
7	chr3:93755817..93758538-chr3:93780645..93782313,2	MCF-7	breast:
8	chr3:93699508..93701266-chr3:93779921..93782891,2	K562	blood:
9	chr3:93700112..93701767-chr3:93770731..93773671,2	K562	blood:
10	chr3:93675612..93678506-chr3:93691202..93693980,2	K562	blood:
11	chr3:93695644..93698458-chr3:93698499..93700134,2	K562	blood:
12	chr3:93753727..93755776-chr3:93757186..93758832,2	K562	blood:
13	chr3:93700627..93702647-chr3:93720581..93722935,2	MCF-7	breast:
14	chr3:93735172..93737336-chr3:93755942..93758232,2	MCF-7	breast:
15	chr3:93743261..93745738-chr3:93780562..93783567,3	MCF-7	breast:
16	chr3:93753727..93755776-chr3:93757186..93758832,2	K562	blood:
17	chr3:93688772..93690676-chr3:93696447..93698454,2	MCF-7	breast:
18	chr3:93691441..93695260-chr3:93696863..93699033,5	MCF-7	breast:
19	chr3:93650076..93652154-chr3:93653341..93655975,2	K562	blood:
20	chr3:93720983..93723390-chr3:93739905..93741891,2	K562	blood:
21	chr3:93644215..93645979-chr3:93647690..93649933,2	K562	blood:
22	chr3:93722699..93725451-chr3:93787826..93790801,2	MCF-7	breast:
23	chr3:93719015..93720527-chr3:93726108..93727920,2	K562	blood:
24	chr3:93722234..93724634-chr3:93733108..93735943,2	K562	blood:
25	chr3:93691277..93692824-chr3:93694719..93696283,2	K562	blood:
26	chr3:93713936..93716429-chr3:93717357..93719541,2	K562	blood:
27	chr3:93695644..93698458-chr3:93698499..93700134,2	K562	blood:
28	chr3:93697861..93699747-chr3:93701242..93703837,2	MCF-7	breast:
29	chr3:93753987..93755557-chr3:93781764..93783415,2	MCF-7	breast:
30	chr3:93690925..93693157-chr3:93696535..93699093,2	MCF-7	breast:
31	chr3:93699718..93702695-chr3:93774813..93776691,2	K562	blood:
32	chr3:93748732..93752259-chr3:93753752..93757151,3	K562	blood:
33	chr3:93682608..93685138-chr3:93687218..93690057,2	K562	blood:
34	chr3:93755277..93756423-chr3:93788135..93789082,3	MCF-7	breast:
35	chr3:93690937..93695495-chr3:93697759..93704969,13	K562	blood:
36	chr3:93739958..93742338-chr3:93782730..93785383,2	K562	blood:
37	chr3:93720544..93724631-chr3:93780488..93783673,7	MCF-7	breast:
38	chr3:93748732..93752259-chr3:93753752..93757151,3	K562	blood:
39	chr3:93721000..93725762-chr3:93785860..93789650,5	MCF-7	breast:
40	chr3:93743036..93744593-chr3:93779189..93782157,2	MCF-7	breast:
41	chr3:93677775..93680053-chr3:93699785..93701689,2	K562	blood:
42	chr16:85780887..85783274-chr3:93688561..93690081,2	MCF-7	breast:
43	chr3:93720983..93723390-chr3:93739905..93741891,2	K562	blood:
44	chr3:93688772..93690676-chr3:93696447..93698454,2	MCF-7	breast:
45	chr3:93686942..93690882-chr3:93698889..93702105,4	K562	blood:
46	chr3:93713936..93716429-chr3:93717357..93719541,2	K562	blood:
47	chr3:93654201..93655762-chr3:93660898..93663750,2	MCF-7	breast:
48	chr3:93719015..93720527-chr3:93726108..93727920,2	K562	blood:
49	chr3:93691277..93692824-chr3:93694719..93696283,2	K562	blood:
50	chr3:93719824..93725075-chr3:93780190..93785120,6	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STX19-1	chr3:93624884-93624987	NONHSAT090718
2	lnc-STX19-1	chr3:93629463-93630001	NONHSAT090718
3	lnc-PROS1-1	chr3:93707478-93707790	NONHSAT090724

No data

Variant related genes	Relation type
HMGN1P7	TF binding region
ENSG00000201339	TF binding region
RNU6-511P	TF binding region
ARL13B	TF binding region
PROS1	TF binding region
STX19	TF binding region
HMGN1P7	CpG island
ENSG00000201339	CpG island
RNU6-511P	CpG island
ARL13B	CpG island
PROS1	CpG island
STX19	CpG island
ENSG00000178700	chromatin interactions
ENSG00000088986	chromatin interactions
ENSG00000184500	chromatin interactions
ENSG00000111786	chromatin interactions
ENSG00000204231	chromatin interactions
ENSG00000272146	chromatin interactions
ENSG00000168374	chromatin interactions
ENSG00000200366	chromatin interactions
ENSG00000169379	chromatin interactions
ENSG00000178694	chromatin interactions
ENSG00000112473	chromatin interactions
ENSG00000201339	chromatin interactions

Extended variants
information (count: 5769 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:5769 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9842413	chr3:93602038-93602039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145895474	chr3:93602182-93602183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533392068	chr3:93602210-93602211	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs576022689	chr3:93602255-93602256	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs542031376	chr3:93602299-93602300	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs377405701	chr3:93602307-93602308	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs556310409	chr3:93602360-93602361	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs561500302	chr3:93602400-93602401	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs527590663	chr3:93602435-93602436	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs540923867	chr3:93602464-93602465	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs369642782	chr3:93602486-93602487	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs372405119	chr3:93602522-93602523	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs577785968	chr3:93602542-93602543	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs545226573	chr3:93602583-93602584	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs549870762	chr3:93602650-93602651	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs553968731	chr3:93602651-93602652	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs570153394	chr3:93602655-93602656	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs572345011	chr3:93602662-93602663	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs549605139	chr3:93602663-93602664	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs375562111	chr3:93602666-93602667	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs188814091	chr3:93602667-93602668	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs535390084	chr3:93602720-93602721	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs558469773	chr3:93602770-93602771	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs181274017	chr3:93602781-93602782	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs541271048	chr3:93602838-93602839	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185269923	chr3:93602913-93602914	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs8178652	chr3:93602927-93602928	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576090743	chr3:93602946-93602947	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147793510	chr3:93602982-93602983	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555188410	chr3:93603011-93603012	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571888084	chr3:93603073-93603074	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540960663	chr3:93603080-93603081	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564420402	chr3:93603104-93603105	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533048494	chr3:93603138-93603139	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543800720	chr3:93603149-93603150	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576340136	chr3:93603155-93603156	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376708845	chr3:93603191-93603192	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529426310	chr3:93603271-93603272	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142552132	chr3:93603272-93603273	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs180849506	chr3:93603275-93603276	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528683534	chr3:93603279-93603280	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551972452	chr3:93603300-93603301	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571931561	chr3:93603365-93603366	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527953885	chr3:93603402-93603403	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187405865	chr3:93603437-93603438	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556134426	chr3:93603451-93603452	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192194033	chr3:93603534-93603535	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199469498	chr3:93603574-93603575	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372203184	chr3:93603588-93603589	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535201753	chr3:93603618-93603619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD

Chromatin state (count:1599 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:93581400-93611000	Weak transcription	Aorta	Aorta
2	chr3:93590400-93602600	Weak transcription	Adipose Nuclei	Adipose
3	chr3:93591000-93610200	Weak transcription	Ovary	ovary
4	chr3:93591000-93614200	Strong transcription	Liver	Liver
5	chr3:93594400-93610600	Weak transcription	Lung	lung
6	chr3:93594600-93632800	Weak transcription	HepG2	liver
7	chr3:93596200-93611000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr3:93597400-93612400	Weak transcription	HSMMtube	muscle
9	chr3:93597400-93629200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr3:93597600-93609800	Weak transcription	Fetal Intestine Small	intestine
11	chr3:93597800-93628800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:93598000-93603000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:93598600-93602200	Weak transcription	Fetal Intestine Large	intestine
14	chr3:93598600-93602600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:93598600-93602800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr3:93601200-93613200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr3:93601800-93625200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr3:93601800-93627200	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr3:93602000-93608400	Weak transcription	Left Ventricle	heart
20	chr3:93602000-93610400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr3:93602200-93603200	ZNF genes & repeats	Fetal Intestine Large	intestine
22	chr3:93602600-93603400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:93602800-93603600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
24	chr3:93603200-93608000	Weak transcription	Fetal Intestine Large	intestine
25	chr3:93603400-93607800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr3:93603600-93609400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr3:93606200-93609600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr3:93606600-93610600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:93607800-93611800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:93608000-93611400	Strong transcription	Fetal Intestine Large	intestine
31	chr3:93608400-93608600	ZNF genes & repeats	Left Ventricle	heart
32	chr3:93608600-93611200	Strong transcription	Left Ventricle	heart
33	chr3:93609000-93625400	Weak transcription	Fetal Stomach	stomach
34	chr3:93609400-93614800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr3:93609600-93612000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:93609800-93611600	Strong transcription	Fetal Intestine Small	intestine
37	chr3:93610200-93612000	Strong transcription	Ovary	ovary
38	chr3:93610400-93636600	Weak transcription	Right Ventricle	heart
39	chr3:93610600-93612000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:93610600-93612000	Strong transcription	Lung	lung
41	chr3:93610800-93611600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr3:93611000-93611200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:93611000-93611400	Strong transcription	Aorta	Aorta
44	chr3:93611200-93625800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr3:93611200-93650400	Weak transcription	Left Ventricle	heart
46	chr3:93611400-93625200	Weak transcription	Fetal Intestine Large	intestine
47	chr3:93611400-93625400	Weak transcription	Aorta	Aorta
48	chr3:93611600-93625200	Weak transcription	Fetal Intestine Small	intestine
49	chr3:93611800-93612200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr3:93612000-93625400	Weak transcription	Lung	lung

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