Variant report

Variant	esv1796952
Chromosome Location	chr8:61492893-61531418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr8:61523592-61523794	K562	blood:	n/a	n/a
2	CBX3	chr8:61517638-61518060	K562	blood:	n/a	n/a
3	CBX3	chr8:61517736-61517998	K562	blood:	n/a	n/a
4	CEBPB	chr8:61496325-61496747	MCF-7	breast:	n/a	n/a
5	CEBPB	chr8:61496425-61496755	IMR90	lung:	n/a	n/a
6	CEBPB	chr8:61496430-61496700	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:61496436-61496730	A549	lung:	n/a	n/a
8	CEBPB	chr8:61526369-61526821	A549	lung:	n/a	n/a
9	CTCF	chr8:61526500-61526650	GM12801	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
10	CTCF	chr8:61523666-61523858	Pancreas_OC	pancreas:	n/a	n/a
11	CTCF	chr8:61523640-61523790	K562	blood:	n/a	n/a
12	CTCF	chr8:61526503-61526672	GM13977	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
13	CTCF	chr8:61523697-61523840	GM10248	blood:	n/a	n/a
14	CTCF	chr8:61523546-61523854	A549	lung:	n/a	n/a
15	CTCF	chr8:61523720-61523870	HL-60	blood:	n/a	n/a
16	CTCF	chr8:61526500-61526650	NB4	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
17	CTCF	chr8:61526500-61526650	AG04450	lung:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
18	CTCF	chr8:61523650-61523880	GM12892	blood:	n/a	n/a
19	CTCF	chr8:61526500-61526650	AG09309	skin:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
20	CTCF	chr8:61523640-61523790	AG04449	skin:	n/a	n/a
21	CTCF	chr8:61526497-61526654	GM10266	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
22	CTCF	chr8:61523660-61523810	GM12874	blood:	n/a	n/a
23	CTCF	chr8:61510024-61510076	GM13976	blood:	n/a	n/a
24	CTCF	chr8:61522060-61522210	K562	blood:	n/a	n/a
25	CTCF	chr8:61526546-61526609	HepG2	liver:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
26	CTCF	chr8:61523660-61523810	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr8:61523540-61523690	NHDF-neo	bronchial:	n/a	n/a
28	CTCF	chr8:61526540-61526690	HCT-116	colon:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
29	CTCF	chr8:61523780-61523930	WI-38	lung:	n/a	n/a
30	CTCF	chr8:61523375-61524016	HCT-116	colon:	n/a	n/a
31	CTCF	chr8:61526480-61526630	NHDF-neo	bronchial:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
32	CTCF	chr8:61526184-61527023	A549	lung:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
33	CTCF	chr8:61526459-61526671	Hela-S3	cervix:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
34	CTCF	chr8:61526840-61526990	GM12870	blood:	n/a	n/a
35	CTCF	chr8:61526381-61526991	SK-N-SH	brain:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
36	CTCF	chr8:61526480-61526630	HBMEC	blood vessel:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
37	CTCF	chr8:61526440-61526590	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr8:61526360-61526510	HVMF	connective:	n/a	n/a
39	CTCF	chr8:61523720-61523870	GM12871	blood:	n/a	n/a
40	CTCF	chr8:61523640-61523790	GM12801	blood:	n/a	n/a
41	CTCF	chr8:61523680-61523830	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:61523720-61523870	GM06990	blood:	n/a	n/a
43	CTCF	chr8:61523620-61523770	GM12865	blood:	n/a	n/a
44	CTCF	chr8:61523660-61523810	AG09319	gingival:	n/a	n/a
45	CTCF	chr8:61523640-61523790	HEK293	kidney:	n/a	n/a
46	CTCF	chr8:61526480-61526630	GM12875	blood:	n/a	chr8:61526583-61526596 chr8:61526585-61526595 chr8:61526582-61526603 chr8:61526581-61526597 chr8:61526580-61526598 chr8:61526583-61526592
47	CTCF	chr8:61523680-61523830	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr8:61523669-61523868	LNCaP	prostate:	n/a	n/a
49	CTCF	chr8:61523720-61523870	HCFaa	heart:	n/a	n/a
50	CTCF	chr8:61523680-61523830	GM12868	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:61496287-61496337	SK-N-SH_RA	brain:	n/a
2	chr8:61496287-61496337	Hela-S3	cervix:	n/a
3	chr8:61496287-61496337	HCM	heart:	n/a
4	chr8:61496287-61496337	Caco-2	colon:	n/a
5	chr8:61496287-61496337	AG10803	skin:	n/a
6	chr8:61496287-61496337	HUVEC	blood vessel:	n/a
7	chr8:61496287-61496337	HMEC	breast:	n/a
8	chr8:61496287-61496337	AG09309	skin:	n/a
9	chr8:61496287-61496337	HEK293	kidney:	embryo
10	chr8:61496287-61496337	H1-hESC	embryonic stem cell:	embryo
11	chr8:61496287-61496337	BJ	skin:	n/a
12	chr8:61496287-61496337	AoSMC	blood vessel:	n/a
13	chr8:61496287-61496337	GM19239	blood:	n/a
14	chr8:61496287-61496337	PrEC	prostate:	n/a
15	chr8:61496287-61496337	ovcar-3	ovarian:	n/a
16	chr8:61496287-61496337	SK-N-MC	brain:	n/a
17	chr8:61496287-61496337	BE2_C	brain:	n/a
18	chr8:61496287-61496337	HRCEpiC	kidney:	n/a
19	chr8:61496287-61496337	K562	blood:	n/a
20	chr8:61496287-61496337	SAEC	small airway:	n/a
21	chr8:61496287-61496337	GM12878	blood:	n/a
22	chr8:61496287-61496337	NH-A	brain:	n/a
23	chr8:61496287-61496337	AG04449	skin:	fetal
24	chr8:61496287-61496337	T-47D	breast:	n/a
25	chr8:61496287-61496337	NB4	blood:	n/a
26	chr8:61496287-61496337	PANC-1	pancreas:	n/a
27	chr8:61496287-61496337	U87	brain:	n/a
28	chr8:61496287-61496337	RPTEC	kidney:	n/a
29	chr8:61496287-61496337	Hepatocyte	liver:	n/a
30	chr8:61496287-61496337	MCF10A-Er-Src	breast:	n/a
31	chr8:61496287-61496337	SK-N-SH	brain:	n/a
32	chr8:61496287-61496337	HRE	kidney:	n/a
33	chr8:61496287-61496337	GM12891	blood:	n/a
34	chr8:61496287-61496337	HL-60	blood:	n/a
35	chr8:61496287-61496337	ProgFib	skin:	n/a
36	chr8:61496287-61496337	GM06990	blood:	n/a
37	chr8:61496287-61496337	Jurkat	blood:	n/a
38	chr8:61496287-61496337	HepG2	liver:	n/a
39	chr8:61496287-61496337	HEEpiC	esophagus:	n/a
40	chr8:61496287-61496337	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:61496287-61496337	A549	lung:	n/a
42	chr8:61496287-61496337	AG09319	gingival:	n/a
43	chr8:61496287-61496337	NT2-D1	testis:	n/a
44	chr8:61496287-61496337	HCT-116	colon:	n/a
45	chr8:61496287-61496337	MCF-7	breast:	n/a
46	chr8:61496287-61496337	NHDF-neo	bronchial:	n/a
47	chr8:61496287-61496337	LNCaP	prostate:	n/a
48	chr8:61496287-61496337	HIPEpiC	eye:	n/a
49	chr8:61496287-61496337	PFSK-1	brain:	n/a
50	chr8:61496287-61496337	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:61324855..61325726-chr8:61523264..61524233,4	MCF-7	breast:
2	chr8:61519878..61522634-chr8:61564445..61566821,2	MCF-7	breast:
3	chr8:61524875..61526902-chr8:61529551..61531219,2	K562	blood:
4	chr8:61428598..61430865-chr8:61522544..61524391,2	MCF-7	breast:
5	chr8:61324832..61325643-chr8:61526141..61526863,2	MCF-7	breast:
6	chr8:61479439..61481118-chr8:61492027..61494400,2	K562	blood:
7	chr8:61494128..61496652-chr8:61499628..61502002,2	MCF-7	breast:
8	chr8:61530201..61533148-chr8:61561938..61565788,3	K562	blood:
9	chr8:61527800..61530109-chr8:61531903..61534207,2	K562	blood:
10	chr8:61524875..61526902-chr8:61529551..61531219,2	K562	blood:
11	chr8:61499691..61501377-chr8:61506333..61508356,2	MCF-7	breast:
12	chr8:61385346..61386405-chr8:61523298..61524048,5	K562	blood:
13	chr8:61525760..61527520-chr8:61863383..61865720,2	K562	blood:
14	chr8:61525465..61527090-chr8:61529519..61532324,2	K562	blood:
15	chr8:61525465..61527090-chr8:61529519..61532324,2	K562	blood:
16	chr8:61511100..61513643-chr8:61515847..61518764,3	MCF-7	breast:
17	chr8:61520531..61524778-chr8:61525857..61529848,4	K562	blood:
18	chr8:61324681..61325874-chr8:61523253..61524359,7	K562	blood:
19	chr8:61521815..61524778-chr8:61526470..61529848,3	K562	blood:
20	chr8:61385902..61386459-chr8:61523291..61524223,2	MCF-7	breast:
21	chr8:61525459..61529300-chr8:61532493..61534738,4	K562	blood:
22	chr8:61490038..61491609-chr8:61491696..61493225,2	K562	blood:
23	chr8:61506351..61508434-chr8:61511898..61514412,2	K562	blood:
24	chr8:61491953..61494205-chr8:61500253..61502240,2	K562	blood:
25	chr8:61486393..61488900-chr8:61501099..61503900,2	K562	blood:
26	chr8:61525175..61527465-chr8:61536083..61538610,2	K562	blood:
27	chr8:61527789..61530559-chr8:61535884..61538190,2	K562	blood:
28	chr8:61511100..61513643-chr8:61515847..61518764,3	MCF-7	breast:
29	chr8:61499691..61501377-chr8:61506333..61508356,2	MCF-7	breast:
30	chr8:61496184..61498168-chr8:61505119..61506811,2	MCF-7	breast:
31	chr8:61427063..61431145-chr8:61524680..61528238,3	MCF-7	breast:
32	chr8:61521815..61524778-chr8:61526470..61529848,3	K562	blood:
33	chr8:61491953..61494205-chr8:61500253..61502240,2	K562	blood:
34	chr8:60964757..60965301-chr8:61523482..61524287,2	MCF-7	breast:
35	chr8:61520531..61524778-chr8:61525857..61529848,4	K562	blood:
36	chr8:61506351..61508434-chr8:61511898..61514412,2	K562	blood:

Variant related genes	Relation type
RAB2A	TF binding region
RAB2A	CpG island
ENSG00000254869	chromatin interactions
ENSG00000104388	chromatin interactions
ENSG00000251396	chromatin interactions

Extended variants
information (count: 1499 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1499 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7013249	chr8:61492893-61492894	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569153044	chr8:61492908-61492909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs56192263	chr8:61492950-61492951	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs201811996	chr8:61492975-61492976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555211282	chr8:61492986-61492987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368871283	chr8:61493054-61493055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537471171	chr8:61493108-61493109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6993237	chr8:61493130-61493131	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs577527878	chr8:61493180-61493181	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs568331901	chr8:61493183-61493184	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs181569783	chr8:61493268-61493269	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201629291	chr8:61493273-61493274	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187035211	chr8:61493318-61493319	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191888225	chr8:61493360-61493361	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184233849	chr8:61493366-61493367	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145727827	chr8:61493427-61493428	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76943941	chr8:61493459-61493460	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185041015	chr8:61493472-61493473	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189555179	chr8:61493508-61493509	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545948555	chr8:61493557-61493558	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548153211	chr8:61493619-61493620	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138308666	chr8:61493626-61493627	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536880256	chr8:61493634-61493635	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573459358	chr8:61493643-61493644	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141796864	chr8:61493659-61493660	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564278710	chr8:61493660-61493661	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144523656	chr8:61493677-61493678	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545651071	chr8:61493693-61493694	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182205246	chr8:61493694-61493695	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528559180	chr8:61493695-61493696	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186893889	chr8:61493731-61493732	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565363563	chr8:61493789-61493790	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575824889	chr8:61493814-61493815	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577266300	chr8:61493818-61493819	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148484740	chr8:61493874-61493875	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116498006	chr8:61493920-61493921	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs192939529	chr8:61493925-61493926	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs546615131	chr8:61494138-61494139	Weak transcription Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542480750	chr8:61494156-61494157	Weak transcription Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116025736	chr8:61494176-61494177	Weak transcription Strong transcription Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs116369328	chr8:61494202-61494203	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570969425	chr8:61494274-61494275	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539979439	chr8:61494304-61494305	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7829359	chr8:61494331-61494332	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs565373314	chr8:61494423-61494424	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576334336	chr8:61494444-61494445	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs202106202	chr8:61494468-61494469	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76073711	chr8:61494494-61494495	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569697963	chr8:61494505-61494506	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs71557801	chr8:61494506-61494507	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:1341 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61439400-61494600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:61448600-61505400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:61458200-61497000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:61459400-61495800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr8:61466400-61516800	Weak transcription	Stomach Mucosa	stomach
6	chr8:61467200-61515400	Weak transcription	Fetal Brain Male	brain
7	chr8:61469000-61495000	Weak transcription	Brain Germinal Matrix	brain
8	chr8:61473600-61493800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr8:61473600-61495000	Weak transcription	Spleen	Spleen
10	chr8:61473600-61497800	Weak transcription	Lung	lung
11	chr8:61474200-61504000	Weak transcription	Colon Smooth Muscle	Colon
12	chr8:61474600-61496200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr8:61474600-61496400	Weak transcription	Thymus	Thymus
14	chr8:61474800-61496000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr8:61474800-61504000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr8:61475000-61493600	Weak transcription	Fetal Kidney	kidney
17	chr8:61475000-61495600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr8:61475400-61494600	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr8:61475400-61498200	Weak transcription	A549	lung
20	chr8:61476200-61495400	Weak transcription	Hela-S3	cervix
21	chr8:61476200-61504800	Weak transcription	NHLF	lung
22	chr8:61476200-61517000	Weak transcription	Brain Angular Gyrus	brain
23	chr8:61476400-61495400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr8:61476400-61496400	Weak transcription	Brain Substantia Nigra	brain
25	chr8:61476600-61495400	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:61476800-61495200	Weak transcription	Brain Anterior Caudate	brain
27	chr8:61477000-61495000	Weak transcription	Ovary	ovary
28	chr8:61477200-61494600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr8:61477400-61497600	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr8:61477800-61493600	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr8:61477800-61496400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr8:61480800-61496600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr8:61481000-61496800	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr8:61481000-61497800	Weak transcription	Gastric	stomach
35	chr8:61481000-61527400	Weak transcription	Psoas Muscle	Psoas
36	chr8:61481200-61504200	Weak transcription	HMEC	breast
37	chr8:61482200-61496200	Weak transcription	Brain Hippocampus Middle	brain
38	chr8:61482800-61496400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr8:61482800-61498000	Weak transcription	Aorta	Aorta
40	chr8:61482800-61504000	Weak transcription	HSMMtube	muscle
41	chr8:61482800-61505800	Weak transcription	Esophagus	oesophagus
42	chr8:61483000-61495000	Weak transcription	Pancreas	Pancrea
43	chr8:61483000-61501200	Weak transcription	NHEK	skin
44	chr8:61483400-61505800	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr8:61483600-61493400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:61483600-61496400	Weak transcription	HUVEC	blood vessel
47	chr8:61483800-61515800	Weak transcription	Colonic Mucosa	Colon
48	chr8:61485400-61515400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr8:61485800-61504400	Weak transcription	Small Intestine	intestine
50	chr8:61486200-61494600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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