Variant report

Variant	nsv948460
Chromosome Location	chr1:175439176-175751385
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2516)
CpG islands
(count:1588)
Chromatin interactive
region (count:86)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2516 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:175677993-175678220	K562	blood:	n/a	n/a
2	ARID3A	chr1:175712067-175712270	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:175450223-175450578	K562	blood:	n/a	n/a
4	ATF1	chr1:175530746-175530820	K562	blood:	n/a	n/a
5	ATF1	chr1:175694946-175695151	K562	blood:	n/a	n/a
6	ATF1	chr1:175440318-175440593	K562	blood:	n/a	n/a
7	ATF1	chr1:175567614-175567771	K562	blood:	n/a	n/a
8	ATF1	chr1:175560566-175560845	K562	blood:	n/a	n/a
9	ATF1	chr1:175702938-175703247	K562	blood:	n/a	n/a
10	ATF2	chr1:175569870-175570603	GM12878	blood:	n/a	n/a
11	ATF2	chr1:175567113-175567630	GM12878	blood:	n/a	n/a
12	ATF2	chr1:175546050-175546351	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr1:175567111-175567613	GM12878	blood:	n/a	n/a
14	BACH1	chr1:175712123-175712541	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr1:175601806-175602145	GM12878	blood:	n/a	chr1:175601977-175601988
16	BATF	chr1:175601811-175602154	GM12878	blood:	n/a	chr1:175601977-175601988
17	BATF	chr1:175570238-175570573	GM12878	blood:	n/a	n/a
18	BATF	chr1:175570278-175570496	GM12878	blood:	n/a	n/a
19	BATF	chr1:175440148-175440454	GM12878	blood:	n/a	chr1:175440280-175440291
20	BATF	chr1:175567105-175567461	GM12878	blood:	n/a	n/a
21	BATF	chr1:175567143-175567484	GM12878	blood:	n/a	n/a
22	BATF	chr1:175659507-175659689	GM12878	blood:	n/a	chr1:175659590-175659601
23	BATF	chr1:175659425-175659778	GM12878	blood:	n/a	chr1:175659590-175659601
24	BCL11A	chr1:175545989-175546282	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCLAF1	chr1:175569764-175570602	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:175560446-175560858	K562	blood:	n/a	n/a
27	BHLHE40	chr1:175568409-175568632	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:175570039-175570625	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:175702931-175703343	K562	blood:	n/a	n/a
30	BRCA1	chr1:175440161-175440685	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr1:175560458-175560815	K562	blood:	n/a	n/a
32	CBX3	chr1:175702890-175703263	K562	blood:	n/a	n/a
33	CCNT2	chr1:175560540-175560861	K562	blood:	n/a	n/a
34	CCNT2	chr1:175726668-175726976	K562	blood:	n/a	n/a
35	CCNT2	chr1:175702945-175703389	K562	blood:	n/a	n/a
36	CEBPB	chr1:175702905-175703334	K562	blood:	n/a	n/a
37	CEBPB	chr1:175467218-175467472	A549	lung:	n/a	n/a
38	CEBPB	chr1:175542608-175543006	Hela-S3	cervix:	n/a	chr1:175542813-175542826
39	CEBPB	chr1:175501817-175501821	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr1:175542608-175543055	ECC-1	luminal epithelium:	n/a	chr1:175542813-175542826
41	CEBPB	chr1:175501279-175501481	K562	blood:	n/a	chr1:175501354-175501365 chr1:175501354-175501367 chr1:175501356-175501367
42	CEBPB	chr1:175440085-175440861	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr1:175456170-175456208	IMR90	lung:	n/a	chr1:175456177-175456188
44	CEBPB	chr1:175570730-175570860	K562	blood:	n/a	chr1:175570824-175570835
45	CEBPB	chr1:175570697-175570866	HepG2	liver:	n/a	chr1:175570824-175570835
46	CEBPB	chr1:175716502-175716663	HepG2	liver:	n/a	chr1:175716563-175716574
47	CEBPB	chr1:175505509-175505801	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:175501291-175501501	A549	lung:	n/a	chr1:175501354-175501365 chr1:175501354-175501367 chr1:175501356-175501367
49	CEBPB	chr1:175569846-175570607	GM12878	blood:	n/a	n/a
50	CEBPB	chr1:175542728-175542915	K562	blood:	n/a	chr1:175542813-175542826

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:175525106-175525156	GM06990	blood:	n/a
2	chr1:175565371-175565421	Hepatocyte	liver:	n/a
3	chr1:175525106-175525156	GM06990	blood:	n/a
4	chr1:175565371-175565421	Hepatocyte	liver:	n/a
5	chr1:175474533-175474583	SKMC	muscle:	n/a
6	chr1:175712382-175712432	HL-60	blood:	n/a
7	chr1:175565371-175565421	GM06990	blood:	n/a
8	chr1:175712382-175712432	HPAEpiC	pulmonary alveolar:	n/a
9	chr1:175474471-175474521	HCT-116	colon:	n/a
10	chr1:175474533-175474583	HL-60	blood:	n/a
11	chr1:175571970-175572020	GM12878	blood:	n/a
12	chr1:175683971-175684021	NB4	blood:	n/a
13	chr1:175525986-175526036	HRCEpiC	kidney:	n/a
14	chr1:175474471-175474521	ovcar-3	ovarian:	n/a
15	chr1:175549030-175549080	SK-N-SH_RA	brain:	n/a
16	chr1:175568377-175568427	HEEpiC	esophagus:	n/a
17	chr1:175533566-175533616	MCF10A-Er-Src	breast:	n/a
18	chr1:175712382-175712432	Caco-2	colon:	n/a
19	chr1:175712382-175712432	Hela-S3	cervix:	n/a
20	chr1:175565371-175565421	HAEpiC	amniotic membrane:	n/a
21	chr1:175511259-175511309	AG04449	skin:	fetal
22	chr1:175653121-175653171	MCF10A-Er-Src	breast:	n/a
23	chr1:175683971-175684021	ECC-1	luminal epithelium:	n/a
24	chr1:175568710-175568760	Jurkat	blood:	n/a
25	chr1:175642761-175642811	IMR90	lung:	fetal
26	chr1:175712871-175712921	GM06990	blood:	n/a
27	chr1:175671657-175671707	NHDF-neo	bronchial:	n/a
28	chr1:175474533-175474583	MCF-7	breast:	n/a
29	chr1:175713219-175713269	LNCaP	prostate:	n/a
30	chr1:175568559-175568609	SKMC	muscle:	n/a
31	chr1:175474471-175474521	HRCEpiC	kidney:	n/a
32	chr1:175568559-175568609	GM06990	blood:	n/a
33	chr1:175565371-175565421	HRPEpiC	eye:	n/a
34	chr1:175568710-175568760	SK-N-SH_RA	brain:	n/a
35	chr1:175671657-175671707	MCF10A-Er-Src	breast:	n/a
36	chr1:175653121-175653171	HNPCEpiC	eye:	n/a
37	chr1:175570022-175570072	AG09309	skin:	n/a
38	chr1:175568559-175568609	K562	blood:	n/a
39	chr1:175568559-175568609	AG10803	skin:	n/a
40	chr1:175474533-175474583	ECC-1	luminal epithelium:	n/a
41	chr1:175490611-175490661	HPAEpiC	pulmonary alveolar:	n/a
42	chr1:175474437-175474487	Hela-S3	cervix:	n/a
43	chr1:175642761-175642811	NHDF-neo	bronchial:	n/a
44	chr1:175568216-175568266	NT2-D1	testis:	n/a
45	chr1:175642761-175642811	SAEC	small airway:	n/a
46	chr1:175568216-175568266	NB4	blood:	n/a
47	chr1:175549030-175549080	NT2-D1	testis:	n/a
48	chr1:175642761-175642811	HCM	heart:	n/a
49	chr1:175474533-175474583	NH-A	brain:	n/a
50	chr1:175570022-175570072	T-47D	breast:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:175638168..175641161-chr1:175648590..175650196,2	MCF-7	breast:
2	chr1:175120985..175121765-chr1:175450538..175451369,3	MCF-7	breast:
3	chr1:175572610..175574256-chr1:175575530..175577590,2	MCF-7	breast:
4	chr1:175703408..175708282-chr1:175710356..175712842,4	K562	blood:
5	chr1:175548057..175550584-chr1:175551957..175553666,2	K562	blood:
6	chr1:175450010..175450941-chr1:175813865..175814693,2	MCF-7	breast:
7	chr1:175619703..175621428-chr1:175631712..175633665,2	K562	blood:
8	chr1:175713728..175714591-chr1:175856822..175857663,2	MCF-7	breast:
9	chr1:175515953..175518588-chr1:175527952..175530742,2	MCF-7	breast:
10	chr1:175722601..175724520-chr1:175811862..175813377,2	K562	blood:
11	chr1:175732717..175735663-chr1:175737285..175738902,2	MCF-7	breast:
12	chr1:175742229..175743888-chr1:175748692..175751512,2	K562	blood:
13	chr1:175593287..175595749-chr1:175606302..175608362,2	K562	blood:
14	chr1:175593287..175595749-chr1:175606302..175608362,2	K562	blood:
15	chr1:175474623..175477393-chr1:175480380..175482566,2	MCF-7	breast:
16	chr1:175572610..175574256-chr1:175575530..175577590,2	MCF-7	breast:
17	chr1:175630324..175632456-chr1:175632718..175635511,2	MCF-7	breast:
18	chr1:175616387..175618880-chr1:175622177..175624894,2	MCF-7	breast:
19	chr1:175548057..175550584-chr1:175551957..175553666,2	K562	blood:
20	chr1:175636404..175638015-chr1:175641711..175644234,2	MCF-7	breast:
21	chr1:175514377..175516679-chr1:175519088..175521360,2	K562	blood:
22	chr1:175474623..175477393-chr1:175480380..175482566,2	MCF-7	breast:
23	chr1:175638168..175641161-chr1:175648590..175650196,2	MCF-7	breast:
24	chr1:175514377..175516679-chr1:175519088..175521360,2	K562	blood:
25	chr1:175479902..175482193-chr1:175482223..175485139,2	K562	blood:
26	chr1:175439998..175440746-chr20:52740037..52740572,2	MCF-7	breast:
27	chr1:175596398..175599153-chr1:175609947..175612782,2	K562	blood:
28	chr1:175623612..175626086-chr1:175627280..175629192,2	K562	blood:
29	chr1:175521179..175523999-chr1:175667216..175668901,2	K562	blood:
30	chr1:175684925..175686685-chr1:175703553..175705621,2	K562	blood:
31	chr1:175528817..175531396-chr1:175532065..175533684,2	MCF-7	breast:
32	chr1:175619703..175621428-chr1:175631712..175633665,2	K562	blood:
33	chr1:175345040..175345864-chr1:175500665..175501444,2	MCF-7	breast:
34	chr1:175437981..175439964-chr1:175464237..175467168,2	K562	blood:
35	chr1:175521179..175523999-chr1:175667216..175668901,2	K562	blood:
36	chr1:175636404..175638015-chr1:175641711..175644234,2	MCF-7	breast:
37	chr1:175512204..175514383-chr1:175514961..175517684,2	K562	blood:
38	chr1:175623612..175625312-chr1:175626921..175628780,2	K562	blood:
39	chr1:175514239..175516178-chr1:175518743..175521414,2	MCF-7	breast:
40	chr1:175450058..175450683-chr1:175793398..175794082,2	MCF-7	breast:
41	chr1:175685957..175688244-chr1:175716194..175717776,2	MCF-7	breast:
42	chr1:175732717..175735663-chr1:175737285..175738902,2	MCF-7	breast:
43	chr1:175450085..175451047-chr1:175712257..175712999,4	MCF-7	breast:
44	chr1:175555708..175557465-chr1:175560630..175563099,2	MCF-7	breast:
45	chr1:175623612..175626086-chr1:175627280..175629192,2	K562	blood:
46	chr1:175623253..175625914-chr1:175631373..175633913,2	K562	blood:
47	chr1:175725153..175728054-chr6:53947666..53950173,2	MCF-7	breast:
48	chr1:175502104..175504991-chr1:175505616..175508224,2	MCF-7	breast:
49	chr1:175518429..175521323-chr1:175522798..175524454,2	K562	blood:
50	chr1:175596398..175599153-chr1:175609947..175612782,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFWD2-2	chr1:175507911-175508312	ENSG00000235628.1
2	lnc-TNR-3	chr1:175712362-175712766	NONHSAT007755
3	lnc-TNN-3	chr1:175535772-175537384	NONHSAT007758
4	lnc-TNN-4	chr1:175601928-175602031	NONHSAT007759
5	lnc-TNN-3	chr1:175526124-175526435	NONHSAT007758
6	lnc-TNN-4	chr1:175599198-175599300	NONHSAT007759
7	lnc-TNN-4	chr1:175592606-175592824	NONHSAT007759
8	lnc-RFWD2-2	chr1:175525727-175525954	ENSG00000235628.1
9	lnc-TNN-3	chr1:175526124-175526435	NONHSAT007757
10	lnc-TNR-3	chr1:175497405-175497505	NONHSAT007755
11	lnc-TNN-3	chr1:175531373-175533005	NONHSAT007757
12	lnc-TNR-3	chr1:175712773-175712906	NONHSAT007755
13	lnc-TNR-5	chr1:175629438-175629547	NONHSAT007760
14	lnc-TNN-4	chr1:175587345-175587409	NONHSAT007759

No data

Variant related genes	Relation type
TNR-IT1	TF binding region
TNR	TF binding region
TNR-IT1	CpG island
TNR	CpG island
ENSG00000116147	chromatin interactions
ENSG00000146147	chromatin interactions

Extended variants
information (count: 11726 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:11726 , 50 per page) page: 1 2 3 4 5 6 7 ... 235

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs859369	chr1:175439176-175439177	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369859865	chr1:175439177-175439178	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs538450323	chr1:175439183-175439184	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs142313977	chr1:175439233-175439234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181466993	chr1:175439247-175439248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs75239395	chr1:175439270-175439271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554114771	chr1:175439277-175439278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574363571	chr1:175439293-175439294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543463693	chr1:175439294-175439295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368729079	chr1:175439309-175439310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545465284	chr1:175439344-175439345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115582781	chr1:175439368-175439369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374878786	chr1:175439374-175439375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144579084	chr1:175439445-175439446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560016258	chr1:175439447-175439448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547172257	chr1:175439472-175439473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185607769	chr1:175439521-175439522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147877606	chr1:175439574-175439575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141621364	chr1:175439594-175439595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367780264	chr1:175439599-175439600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150433682	chr1:175439635-175439636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10912987	chr1:175439672-175439673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4652095	chr1:175439692-175439693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537748247	chr1:175439714-175439715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541389401	chr1:175439716-175439717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74127304	chr1:175439750-175439751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs551285428	chr1:175439778-175439779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34228302	chr1:175439788-175439789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565560072	chr1:175439796-175439797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534569484	chr1:175439814-175439815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79226686	chr1:175439827-175439828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189974892	chr1:175439843-175439844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114410006	chr1:175439941-175439942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182666692	chr1:175439955-175439956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576844164	chr1:175439963-175439964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187697704	chr1:175440040-175440041	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs533857684	chr1:175440041-175440042	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs567598081	chr1:175440068-175440069	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs149186260	chr1:175440098-175440099	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs191999244	chr1:175440126-175440127	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs542497373	chr1:175440145-175440146	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs863518	chr1:175440153-175440154	Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs575932243	chr1:175440154-175440155	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs143367954	chr1:175440216-175440217	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115918614	chr1:175440229-175440230	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79767642	chr1:175440251-175440252	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs61808381	chr1:175440252-175440253	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559080378	chr1:175440255-175440256	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528273132	chr1:175440309-175440310	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573301500	chr1:175440310-175440311	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1582 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:175434400-175439200	Weak transcription	Fetal Intestine Large	intestine
2	chr1:175438800-175440000	Enhancers	NHEK	skin
3	chr1:175438800-175442000	Enhancers	Hela-S3	cervix
4	chr1:175439000-175439200	Bivalent Enhancer	HMEC	breast
5	chr1:175439000-175440800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:175439200-175440000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:175439200-175440600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:175439200-175440800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:175439200-175440800	Enhancers	Fetal Intestine Small	intestine
10	chr1:175439200-175440800	Enhancers	HMEC	breast
11	chr1:175439200-175441400	Enhancers	Fetal Intestine Large	intestine
12	chr1:175439400-175440400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:175439400-175441000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr1:175439800-175440200	Enhancers	Brain Angular Gyrus	brain
15	chr1:175439800-175440600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr1:175440000-175440200	Flanking Active TSS	NHEK	skin
17	chr1:175440000-175440400	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr1:175440200-175440400	Enhancers	NHEK	skin
19	chr1:175440400-175440600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr1:175440400-175440600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:175440400-175440600	Flanking Active TSS	NHEK	skin
22	chr1:175440600-175441400	Enhancers	NHEK	skin
23	chr1:175440800-175447000	Weak transcription	Fetal Intestine Small	intestine
24	chr1:175441000-175443800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:175441400-175446400	Weak transcription	Fetal Intestine Large	intestine
26	chr1:175442000-175446400	Weak transcription	Hela-S3	cervix
27	chr1:175443800-175444000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr1:175444000-175445200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:175445200-175445800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr1:175445400-175445800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:175445800-175446800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr1:175446000-175446800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr1:175446400-175447200	Enhancers	Brain Germinal Matrix	brain
34	chr1:175446400-175448400	Enhancers	Hela-S3	cervix
35	chr1:175446400-175451000	Enhancers	Fetal Intestine Large	intestine
36	chr1:175446600-175447800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr1:175446600-175448000	Enhancers	Fetal Brain Male	brain
38	chr1:175446800-175447400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:175446800-175447600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:175446800-175447600	Enhancers	Aorta	Aorta
41	chr1:175446800-175447800	Enhancers	Fetal Brain Female	brain
42	chr1:175447000-175447600	Enhancers	Stomach Smooth Muscle	stomach
43	chr1:175447000-175448800	Enhancers	Fetal Intestine Small	intestine
44	chr1:175447200-175447800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:175447200-175454200	Weak transcription	Brain Germinal Matrix	brain
46	chr1:175447400-175447600	Bivalent Enhancer	Fetal Lung	lung
47	chr1:175447400-175448400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr1:175447600-175449200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:175447800-175448000	Bivalent Enhancer	NH-A	brain
50	chr1:175447800-175448200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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