Variant report

Variant	nsv916541
Chromosome Location	chr3:93575289-93758589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1599)
CpG islands
(count:1954)
Chromatin interactive
region (count:81)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:93676282-93676501	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:93690348-93690789	K562	blood:	n/a	n/a
3	ARID3A	chr3:93692592-93692986	K562	blood:	n/a	n/a
4	ARID3A	chr3:93642022-93642172	K562	blood:	n/a	n/a
5	ARID3A	chr3:93698649-93699202	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:93691767-93692970	HepG2	liver:	n/a	n/a
7	ATF1	chr3:93698620-93699143	K562	blood:	n/a	n/a
8	ATF1	chr3:93688928-93689209	K562	blood:	n/a	n/a
9	ATF1	chr3:93692661-93693084	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	chr3:93690516-93690676	K562	blood:	n/a	n/a
17	BHLHE40	chr3:93692454-93693052	K562	blood:	n/a	n/a
18	BHLHE40	chr3:93698432-93699352	K562	blood:	n/a	n/a
19	BHLHE40	chr3:93688299-93688633	K562	blood:	n/a	n/a
20	BHLHE40	chr3:93698741-93699514	GM12878	blood:	n/a	n/a
21	BRCA1	chr3:93698957-93699082	HepG2	liver:	n/a	n/a
22	BRCA1	chr3:93698708-93699567	Hela-S3	cervix:	n/a	chr3:93699508-93699515
23	BRCA1	chr3:93692300-93692913	HepG2	liver:	n/a	n/a
24	CBX3	chr3:93625948-93626194	K562	blood:	n/a	n/a
25	CBX3	chr3:93700392-93700721	K562	blood:	n/a	n/a
26	CBX3	chr3:93660944-93661275	K562	blood:	n/a	n/a
27	CBX3	chr3:93661017-93661284	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	chr3:93692423-93693063	K562	blood:	n/a	chr3:93692940-93692949
31	CCNT2	chr3:93688880-93689213	K562	blood:	n/a	n/a
32	CEBPB	chr3:93693229-93693381	K562	blood:	n/a	n/a
33	CEBPB	chr3:93704056-93704242	K562	blood:	n/a	chr3:93704193-93704206
34	CEBPB	chr3:93698943-93699110	HepG2	liver:	n/a	n/a
35	CEBPB	chr3:93577008-93577134	A549	lung:	n/a	n/a
36	CEBPB	chr3:93688933-93689299	K562	blood:	n/a	n/a
37	CEBPB	chr3:93615540-93615692	K562	blood:	n/a	chr3:93615585-93615598
38	CEBPB	chr3:93649629-93649633	K562	blood:	n/a	n/a
39	CEBPB	chr3:93700376-93700715	K562	blood:	n/a	n/a
40	CEBPB	chr3:93716756-93716887	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr3:93650673-93650708	K562	blood:	n/a	chr3:93650686-93650699 chr3:93650686-93650697
42	CEBPB	chr3:93683888-93684166	A549	lung:	n/a	chr3:93684037-93684048
43	CEBPB	chr3:93629003-93629273	HepG2	liver:	n/a	chr3:93629160-93629171 chr3:93629159-93629172 chr3:93629159-93629170
44	CEBPB	chr3:93650513-93650709	HepG2	liver:	n/a	chr3:93650686-93650699 chr3:93650686-93650697
45	CEBPB	chr3:93736618-93736843	K562	blood:	n/a	chr3:93736693-93736704
46	CEBPB	chr3:93690689-93691261	K562	blood:	n/a	chr3:93690752-93690765 chr3:93690752-93690765 chr3:93691136-93691147 chr3:93691136-93691147
47	CEBPB	chr3:93736580-93736799	HepG2	liver:	n/a	chr3:93736693-93736704
48	CEBPB	chr3:93691906-93692431	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:93683932-93684221	HepG2	liver:	n/a	chr3:93684037-93684048
50	CEBPB	chr3:93692007-93692174	HepG2	liver:	n/a	n/a

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:93702658-93702708	PANC-1	pancreas:	n/a
2	chr3:93592719-93592769	PANC-1	pancreas:	n/a
3	chr3:93702658-93702708	PANC-1	pancreas:	n/a
4	chr3:93592719-93592769	PANC-1	pancreas:	n/a
5	chr3:93698768-93698818	AG10803	skin:	n/a
6	chr3:93698932-93698982	NHDF-neo	bronchial:	n/a
7	chr3:93747410-93747460	HEEpiC	esophagus:	n/a
8	chr3:93692764-93692814	PFSK-1	brain:	n/a
9	chr3:93698939-93698989	SK-N-SH_RA	brain:	n/a
10	chr3:93698864-93698914	Hepatocyte	liver:	n/a
11	chr3:93692764-93692814	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:93698768-93698818	HRCEpiC	kidney:	n/a
13	chr3:93698966-93699016	HCPEpiC	choroid plexus:	n/a
14	chr3:93647605-93647655	SAEC	small airway:	n/a
15	chr3:93698461-93698511	HRE	kidney:	n/a
16	chr3:93692952-93693002	NHDF-neo	bronchial:	n/a
17	chr3:93692952-93693002	A549	lung:	n/a
18	chr3:93647007-93647057	Hela-S3	cervix:	n/a
19	chr3:93698966-93699016	HEEpiC	esophagus:	n/a
20	chr3:93692773-93692823	CMK	blood:	n/a
21	chr3:93699352-93699402	GM12891	blood:	n/a
22	chr3:93692925-93692975	GM12878	blood:	n/a
23	chr3:93696108-93696158	IMR90	lung:	fetal
24	chr3:93698966-93699016	MCF-7	breast:	n/a
25	chr3:93692952-93693002	AG09319	gingival:	n/a
26	chr3:93696108-93696158	NT2-D1	testis:	n/a
27	chr3:93592719-93592769	HCM	heart:	n/a
28	chr3:93698964-93699014	ovcar-3	ovarian:	n/a
29	chr3:93693147-93693197	HEEpiC	esophagus:	n/a
30	chr3:93647007-93647057	HL-60	blood:	n/a
31	chr3:93646432-93646482	SKMC	muscle:	n/a
32	chr3:93646378-93646428	MCF10A-Er-Src	breast:	n/a
33	chr3:93698231-93698281	Caco-2	colon:	n/a
34	chr3:93699019-93699069	HUVEC	blood vessel:	n/a
35	chr3:93698966-93699016	NHBE	bronchial:	n/a
36	chr3:93689422-93689472	Hepatocyte	liver:	n/a
37	chr3:93702658-93702708	HIPEpiC	eye:	n/a
38	chr3:93692773-93692823	ovcar-3	ovarian:	n/a
39	chr3:93699352-93699402	MCF-7	breast:	n/a
40	chr3:93692564-93692614	Jurkat	blood:	n/a
41	chr3:93699352-93699402	PrEC	prostate:	n/a
42	chr3:93592719-93592769	HNPCEpiC	eye:	n/a
43	chr3:93747528-93747578	NT2-D1	testis:	n/a
44	chr3:93747410-93747460	NH-A	brain:	n/a
45	chr3:93699352-93699402	HRCEpiC	kidney:	n/a
46	chr3:93698461-93698511	AG09309	skin:	n/a
47	chr3:93733689-93733739	ovcar-3	ovarian:	n/a
48	chr3:93647007-93647057	HUVEC	blood vessel:	n/a
49	chr3:93698928-93698978	SK-N-MC	brain:	n/a
50	chr3:93698533-93698583	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:93686942..93690882-chr3:93698889..93702105,4	K562	blood:
2	chr3:93688772..93690676-chr3:93696447..93698454,2	MCF-7	breast:
3	chr3:93644215..93645979-chr3:93647690..93649933,2	K562	blood:
4	chr3:93685719..93688188-chr3:93691422..93694022,3	MCF-7	breast:
5	chr3:93722234..93724634-chr3:93733108..93735943,2	K562	blood:
6	chr3:93691441..93695260-chr3:93696863..93699033,5	MCF-7	breast:
7	chr3:93743036..93744593-chr3:93779189..93782157,2	MCF-7	breast:
8	chr3:93722817..93723819-chr3:93787860..93788816,4	MCF-7	breast:
9	chr3:93699087..93699759-chr6:33167964..33168678,2	Hela-S3	cervix:
10	chr3:93675612..93678506-chr3:93691202..93693980,2	K562	blood:
11	chr3:93720983..93723390-chr3:93739905..93741891,2	K562	blood:
12	chr3:93708802..93710855-chr3:93729063..93731672,2	MCF-7	breast:
13	chr3:93713936..93716429-chr3:93717357..93719541,2	K562	blood:
14	chr3:93721000..93725762-chr3:93785860..93789650,5	MCF-7	breast:
15	chr3:93690937..93695495-chr3:93697759..93704969,13	K562	blood:
16	chr3:93677775..93680053-chr3:93699785..93701689,2	K562	blood:
17	chr3:93725914..93728188-chr3:93784613..93787224,2	K562	blood:
18	chr3:93699718..93702695-chr3:93774813..93776691,2	K562	blood:
19	chr3:93755817..93758538-chr3:93780645..93782313,2	MCF-7	breast:
20	chr3:93614459..93614996-chr5:160095807..160096625,2	MCF-7	breast:
21	chr3:93571786..93573423-chr3:93699770..93701438,2	K562	blood:
22	chr3:93690925..93693157-chr3:93696535..93699093,2	MCF-7	breast:
23	chr3:93722234..93724634-chr3:93733108..93735943,2	K562	blood:
24	chr3:93755277..93756423-chr3:93788135..93789082,3	MCF-7	breast:
25	chr3:93719015..93720527-chr3:93726108..93727920,2	K562	blood:
26	chr3:93720983..93723390-chr3:93739905..93741891,2	K562	blood:
27	chr3:93654201..93655762-chr3:93660898..93663750,2	MCF-7	breast:
28	chr3:93699508..93701266-chr3:93779921..93782891,2	K562	blood:
29	chr3:93720544..93724631-chr3:93780488..93783673,7	MCF-7	breast:
30	chr3:93700112..93701767-chr3:93770731..93773671,2	K562	blood:
31	chr3:93650076..93652154-chr3:93653341..93655975,2	K562	blood:
32	chr3:93690937..93695495-chr3:93697759..93704969,13	K562	blood:
33	chr3:93719824..93725075-chr3:93780190..93785120,6	MCF-7	breast:
34	chr3:93686048..93689439-chr3:93690333..93693840,4	K562	blood:
35	chr3:93735172..93737336-chr3:93755942..93758232,2	MCF-7	breast:
36	chr3:93722902..93723801-chr3:93787301..93788704,3	K562	blood:
37	chr3:93677775..93680053-chr3:93699785..93701689,2	K562	blood:
38	chr3:93748732..93752259-chr3:93753752..93757151,3	K562	blood:
39	chr3:93666897..93669716-chr3:93698788..93701503,2	K562	blood:
40	chr3:93695644..93698458-chr3:93698499..93700134,2	K562	blood:
41	chr3:93690925..93693157-chr3:93696535..93699093,2	MCF-7	breast:
42	chr3:93679066..93682054-chr3:93685167..93688192,3	K562	blood:
43	chr3:93722783..93723665-chr3:93787777..93788798,5	MCF-7	breast:
44	chr3:93743261..93745738-chr3:93780562..93783567,3	MCF-7	breast:
45	chr3:93745389..93747015-chr3:93779840..93782675,2	MCF-7	breast:
46	chr3:93666583..93669103-chr3:93690628..93693616,3	MCF-7	breast:
47	chr3:93742669..93744439-chr3:93784562..93786403,2	MCF-7	breast:
48	chr3:93723191..93723797-chr3:93786247..93787199,2	MCF-7	breast:
49	chr3:93713936..93716429-chr3:93717357..93719541,2	K562	blood:
50	chr3:93686048..93689439-chr3:93690333..93693840,4	K562	blood:

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

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

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PROS1	hsa-miR-335-5p	chr3:93592888-93592909

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

Extended variants
information (count: 6692 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:6692 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553625692	chr3:93575356-93575357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs375367336	chr3:93575367-93575368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186571756	chr3:93575421-93575422	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189444428	chr3:93575424-93575425	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558977852	chr3:93575443-93575444	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554787380	chr3:93575444-93575445	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543028949	chr3:93575452-93575453	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181818291	chr3:93575512-93575513	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140945243	chr3:93575513-93575514	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576138414	chr3:93575531-93575532	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542285281	chr3:93575558-93575559	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559123881	chr3:93575607-93575608	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9682417	chr3:93575648-93575649	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs551692324	chr3:93575678-93575679	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76993057	chr3:93575716-93575717	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571431928	chr3:93575718-93575719	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530971429	chr3:93575720-93575721	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186894541	chr3:93575735-93575736	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567626179	chr3:93575809-93575810	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150186041	chr3:93575830-93575831	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553465020	chr3:93575834-93575835	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs145763148	chr3:93575836-93575837	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539233587	chr3:93575850-93575851	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559229879	chr3:93575858-93575859	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575832584	chr3:93575885-93575886	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191435694	chr3:93575889-93575890	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556704140	chr3:93575947-93575948	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs576699923	chr3:93575971-93575972	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573253322	chr3:93576024-93576025	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542320286	chr3:93576089-93576090	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559012502	chr3:93576156-93576157	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528301663	chr3:93576205-93576206	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544863203	chr3:93576217-93576218	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374310369	chr3:93576228-93576229	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112934758	chr3:93576273-93576274	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376934608	chr3:93576284-93576285	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530738895	chr3:93576291-93576292	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550805028	chr3:93576294-93576295	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567673887	chr3:93576321-93576322	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541030542	chr3:93576437-93576438	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530110134	chr3:93576449-93576450	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547163113	chr3:93576482-93576483	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566948322	chr3:93576545-93576546	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539269029	chr3:93576553-93576554	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552511273	chr3:93576587-93576588	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115011661	chr3:93576625-93576626	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574633611	chr3:93576649-93576650	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541954980	chr3:93576653-93576654	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183353397	chr3:93576717-93576718	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545214038	chr3:93576770-93576771	ZNF genes & repeats Weak 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:1645 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:93574800-93576200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:93575400-93579400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
3	chr3:93576200-93576600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:93576600-93578200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr3:93578200-93581400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:93581200-93581400	Enhancers	Aorta	Aorta
7	chr3:93581400-93582400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:93581400-93611000	Weak transcription	Aorta	Aorta
9	chr3:93582400-93582800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:93586400-93586600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:93588600-93589800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr3:93589000-93600000	Weak transcription	Left Ventricle	heart
13	chr3:93589400-93591000	Weak transcription	Liver	Liver
14	chr3:93589800-93595800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr3:93590400-93602600	Weak transcription	Adipose Nuclei	Adipose
16	chr3:93591000-93610200	Weak transcription	Ovary	ovary
17	chr3:93591000-93614200	Strong transcription	Liver	Liver
18	chr3:93592000-93595000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr3:93594400-93597000	Weak transcription	Psoas Muscle	Psoas
20	chr3:93594400-93610600	Weak transcription	Lung	lung
21	chr3:93594600-93632800	Weak transcription	HepG2	liver
22	chr3:93595000-93595800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr3:93595800-93596000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:93595800-93597000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr3:93596000-93596200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr3:93596200-93598600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:93596200-93611000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:93596400-93596800	Enhancers	HMEC	breast
29	chr3:93596400-93598000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:93596400-93598200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr3:93596600-93597000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
32	chr3:93596600-93597400	Enhancers	HSMMtube	muscle
33	chr3:93596600-93597400	Enhancers	NHEK	skin
34	chr3:93596600-93597800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:93596600-93598000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr3:93596800-93597000	Flanking Active TSS	HMEC	breast
37	chr3:93596800-93597800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr3:93596800-93598200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr3:93597000-93597400	Active TSS	HMEC	breast
40	chr3:93597000-93597600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr3:93597000-93598000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr3:93597000-93598400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr3:93597400-93597600	Flanking Active TSS	HMEC	breast
44	chr3:93597400-93597800	Flanking Active TSS	NHEK	skin
45	chr3:93597400-93612400	Weak transcription	HSMMtube	muscle
46	chr3:93597400-93629200	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr3:93597600-93598200	Enhancers	HMEC	breast
48	chr3:93597600-93609800	Weak transcription	Fetal Intestine Small	intestine
49	chr3:93597800-93598000	Enhancers	NHEK	skin
50	chr3:93597800-93628800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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