Variant report

Variant	nsv1027585
Chromosome Location	chr8:125627924-125707738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1792)
CpG islands
(count:367)
Chromatin interactive
region (count:217)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1792 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:125648665-125649330	K562	blood:	n/a	n/a
2	ARID3A	chr8:125647631-125647966	K562	blood:	n/a	n/a
3	ARID3A	chr8:125629006-125629324	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:125704619-125704877	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:125663241-125663958	K562	blood:	n/a	n/a
6	ARID3A	chr8:125699777-125700135	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:125696658-125697111	K562	blood:	n/a	n/a
8	ARID3A	chr8:125643175-125644057	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:125628704-125628796	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:125661251-125662149	K562	blood:	n/a	n/a
11	ARID3A	chr8:125641947-125642374	K562	blood:	n/a	chr8:125642351-125642367 chr8:125642352-125642368
12	ARID3A	chr8:125658712-125658714	K562	blood:	n/a	n/a
13	ARID3A	chr8:125659867-125660366	K562	blood:	n/a	n/a
14	ARID3A	chr8:125699950-125700136	K562	blood:	n/a	n/a
15	ARID3A	chr8:125681230-125682877	HepG2	liver:	n/a	chr8:125681477-125681493
16	ARID3A	chr8:125672554-125672908	K562	blood:	n/a	n/a
17	ARID3A	chr8:125640413-125640822	K562	blood:	n/a	n/a
18	ARID3A	chr8:125667701-125668102	HepG2	liver:	n/a	n/a
19	ARID3A	chr8:125707409-125707744	K562	blood:	n/a	n/a
20	ARID3A	chr8:125685882-125685917	K562	blood:	n/a	n/a
21	ARID3A	chr8:125667710-125668084	K562	blood:	n/a	n/a
22	ATF1	chr8:125649782-125650097	K562	blood:	n/a	n/a
23	ATF1	chr8:125667688-125668035	K562	blood:	n/a	n/a
24	ATF1	chr8:125685677-125686000	K562	blood:	n/a	n/a
25	ATF1	chr8:125661336-125662132	K562	blood:	n/a	n/a
26	ATF1	chr8:125647584-125647987	K562	blood:	n/a	n/a
27	ATF1	chr8:125672571-125673078	K562	blood:	n/a	n/a
28	ATF1	chr8:125663333-125663983	K562	blood:	n/a	n/a
29	ATF1	chr8:125641890-125642377	K562	blood:	n/a	n/a
30	ATF2	chr8:125656159-125656732	GM12878	blood:	n/a	n/a
31	ATF2	chr8:125641781-125642341	GM12878	blood:	n/a	n/a
32	ATF2	chr8:125685564-125686080	GM12878	blood:	n/a	n/a
33	ATF2	chr8:125649640-125650283	GM12878	blood:	n/a	n/a
34	ATF2	chr8:125685580-125686052	GM12878	blood:	n/a	n/a
35	ATF2	chr8:125700782-125701335	GM12878	blood:	n/a	n/a
36	ATF2	chr8:125681294-125681727	GM12878	blood:	n/a	n/a
37	ATF2	chr8:125649592-125650379	GM12878	blood:	n/a	n/a
38	ATF2	chr8:125641749-125642412	GM12878	blood:	n/a	n/a
39	ATF2	chr8:125653018-125653514	GM12878	blood:	n/a	n/a
40	ATF2	chr8:125653011-125653451	GM12878	blood:	n/a	n/a
41	ATF3	chr8:125663416-125663683	K562	blood:	n/a	n/a
42	ATF3	chr8:125663272-125663735	K562	blood:	n/a	n/a
43	ATF3	chr8:125642108-125642270	K562	blood:	n/a	chr8:125642236-125642250
44	ATF3	chr8:125641985-125642349	K562	blood:	n/a	chr8:125642236-125642250
45	ATF3	chr8:125685643-125685968	K562	blood:	n/a	n/a
46	ATF3	chr8:125638999-125639252	K562	blood:	n/a	n/a
47	BACH1	chr8:125642060-125642390	K562	blood:	n/a	chr8:125642173-125642187
48	BACH1	chr8:125648797-125649445	K562	blood:	n/a	n/a
49	BACH1	chr8:125663346-125663689	K562	blood:	n/a	n/a
50	BATF	chr8:125649660-125650149	GM12878	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:125640145-125640195	SK-N-SH	brain:	n/a
2	chr8:125640145-125640195	SK-N-SH	brain:	n/a
3	chr8:125678187-125678237	AG09309	skin:	n/a
4	chr8:125699897-125699947	SKMC	muscle:	n/a
5	chr8:125631251-125631301	PANC-1	pancreas:	n/a
6	chr8:125678187-125678237	LNCaP	prostate:	n/a
7	chr8:125640145-125640195	NH-A	brain:	n/a
8	chr8:125699897-125699947	HRE	kidney:	n/a
9	chr8:125631251-125631301	BJ	skin:	n/a
10	chr8:125678187-125678237	HUVEC	blood vessel:	n/a
11	chr8:125642769-125642819	HCF	heart:	n/a
12	chr8:125699897-125699947	IMR90	lung:	fetal
13	chr8:125631251-125631301	T-47D	breast:	n/a
14	chr8:125672795-125672845	MCF10A-Er-Src	breast:	n/a
15	chr8:125672795-125672845	NHDF-neo	bronchial:	n/a
16	chr8:125631251-125631301	HL-60	blood:	n/a
17	chr8:125699897-125699947	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:125640145-125640195	LNCaP	prostate:	n/a
19	chr8:125678187-125678237	ovcar-3	ovarian:	n/a
20	chr8:125672795-125672845	HEEpiC	esophagus:	n/a
21	chr8:125699897-125699947	GM12891	blood:	n/a
22	chr8:125672795-125672845	Hela-S3	cervix:	n/a
23	chr8:125678187-125678237	MCF-7	breast:	n/a
24	chr8:125672795-125672845	BE2_C	brain:	n/a
25	chr8:125678187-125678237	HCT-116	colon:	n/a
26	chr8:125642769-125642819	HAEpiC	amniotic membrane:	n/a
27	chr8:125640145-125640195	AG04450	lung:	fetal
28	chr8:125678187-125678237	NT2-D1	testis:	n/a
29	chr8:125642769-125642819	NB4	blood:	n/a
30	chr8:125672795-125672845	HepG2	liver:	n/a
31	chr8:125678187-125678237	K562	blood:	n/a
32	chr8:125640145-125640195	ECC-1	luminal epithelium:	n/a
33	chr8:125678187-125678237	HCF	heart:	n/a
34	chr8:125678187-125678237	HEEpiC	esophagus:	n/a
35	chr8:125672795-125672845	HRCEpiC	kidney:	n/a
36	chr8:125678187-125678237	NHDF-neo	bronchial:	n/a
37	chr8:125642769-125642819	BJ	skin:	n/a
38	chr8:125678187-125678237	A549	lung:	n/a
39	chr8:125642769-125642819	GM06990	blood:	n/a
40	chr8:125699897-125699947	HRCEpiC	kidney:	n/a
41	chr8:125631251-125631301	U87	brain:	n/a
42	chr8:125640145-125640195	IMR90	lung:	fetal
43	chr8:125642769-125642819	NH-A	brain:	n/a
44	chr8:125699897-125699947	SK-N-SH_RA	brain:	n/a
45	chr8:125672795-125672845	U87	brain:	n/a
46	chr8:125631251-125631301	NH-A	brain:	n/a
47	chr8:125640145-125640195	HRE	kidney:	n/a
48	chr8:125699897-125699947	HEK293	kidney:	embryo
49	chr8:125640145-125640195	HL-60	blood:	n/a
50	chr8:125672795-125672845	IMR90	lung:	fetal

(count:217 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:125647705..125651624-chr8:125656720..125658741,4	K562	blood:
2	chr8:125639927..125641909-chr8:125654623..125657042,2	MCF-7	breast:
3	chr8:125663736..125665496-chr8:125671253..125674701,3	MCF-7	breast:
4	chr8:125704431..125707211-chr8:125707702..125710134,3	K562	blood:
5	chr8:125672360..125675088-chr8:125677995..125680421,2	K562	blood:
6	chr8:125644080..125646951-chr8:125648731..125650374,2	MCF-7	breast:
7	chr8:125657106..125660493-chr8:125825851..125829394,4	K562	blood:
8	chr8:125642370..125644650-chr8:125657174..125658829,2	K562	blood:
9	chr8:125685458..125688128-chr8:125691791..125694776,4	K562	blood:
10	chr8:125699774..125701577-chr8:125704384..125706753,2	K562	blood:
11	chr8:125617943..125619581-chr8:125634142..125635689,2	MCF-7	breast:
12	chr8:125640772..125642364-chr8:125869019..125870864,2	MCF-7	breast:
13	chr8:125658235..125661140-chr8:125662893..125664695,2	K562	blood:
14	chr8:125664797..125667579-chr8:125686939..125689871,2	K562	blood:
15	chr8:125574370..125578079-chr8:125630160..125632086,3	MCF-7	breast:
16	chr8:125627308..125630217-chr8:125638327..125642424,3	K562	blood:
17	chr8:125629075..125631557-chr8:125633717..125635693,2	K562	blood:
18	chr8:125673813..125676349-chr8:125984209..125986396,2	MCF-7	breast:
19	chr8:125549859..125552805-chr8:125642129..125643767,2	MCF-7	breast:
20	chr8:125638065..125640378-chr8:125640492..125642045,2	K562	blood:
21	chr8:125604891..125605818-chr8:125659721..125660571,4	K562	blood:
22	chr1:181367510..181368414-chr8:125631724..125632371,2	MCF-7	breast:
23	chr8:125634912..125639122-chr8:125652761..125656973,4	K562	blood:
24	chr8:125680861..125685703-chr8:125685975..125688840,5	MCF-7	breast:
25	chr8:125623032..125625031-chr8:125629309..125631015,2	K562	blood:
26	chr8:125676205..125678363-chr8:125679206..125681734,2	MCF-7	breast:
27	chr8:125549825..125551523-chr8:125704908..125707139,2	MCF-7	breast:
28	chr8:125648801..125651687-chr8:125651691..125654653,2	MCF-7	breast:
29	chr8:125667582..125669252-chr8:125725497..125727045,2	MCF-7	breast:
30	chr8:125628049..125629556-chr8:125636539..125638565,2	MCF-7	breast:
31	chr8:125638351..125644610-chr8:125826258..125829486,6	K562	blood:
32	chr8:125658978..125663524-chr8:125664698..125669211,7	MCF-7	breast:
33	chr8:125650533..125653150-chr8:125663806..125665478,2	MCF-7	breast:
34	chr8:125650533..125653150-chr8:125663806..125665478,2	MCF-7	breast:
35	chr8:125604259..125604772-chr8:125659807..125660340,2	MCF-7	breast:
36	chr8:125654604..125657235-chr8:125659497..125661452,3	K562	blood:
37	chr8:125665987..125668310-chr8:125675466..125678382,3	K562	blood:
38	chr8:125663706..125665321-chr8:125671326..125673228,2	K562	blood:
39	chr8:125662479..125664337-chr8:125697312..125699450,2	MCF-7	breast:
40	chr8:125653582..125656116-chr8:125824961..125827801,3	K562	blood:
41	chr8:125636931..125639466-chr8:125722447..125724460,2	MCF-7	breast:
42	chr8:125673153..125675208-chr8:125677038..125679927,4	MCF-7	breast:
43	chr8:125685948..125687949-chr8:125826309..125828917,3	K562	blood:
44	chr8:125640852..125644024-chr8:125644604..125648826,4	MCF-7	breast:
45	chr8:125703204..125704827-chr8:125704961..125706579,2	MCF-7	breast:
46	chr8:125659876..125664799-chr8:125825896..125829544,9	K562	blood:
47	chr8:125658978..125663524-chr8:125664698..125669211,7	MCF-7	breast:
48	chr8:125642370..125644650-chr8:125657174..125658829,2	K562	blood:
49	chr8:125675687..125677543-chr8:125681437..125683937,2	K562	blood:
50	chr8:125697915..125700956-chr8:125703472..125706654,3	K562	blood:

No data

Variant related genes	Relation type
MTSS1	TF binding region
MTSS1	CpG island
ENSG00000180938	chromatin interactions
ENSG00000255491	chromatin interactions
ENSG00000249816	chromatin interactions
ENSG00000147684	chromatin interactions
ENSG00000005700	chromatin interactions
ENSG00000272486	chromatin interactions
ENSG00000147687	chromatin interactions
ENSG00000255080	chromatin interactions
ENSG00000170873	chromatin interactions
ENSG00000056736	chromatin interactions
ENSG00000016391	chromatin interactions

Extended variants
information (count: 3264 )
Associated
traits (count: 147 )

Variant overlapped rSNPs/rCNVs (count:3264 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16893079	chr8:125627924-125627925	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147515154	chr8:125627925-125627926	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs62530670	chr8:125627950-125627951	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs113735498	chr8:125627970-125627971	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs564901932	chr8:125627971-125627972	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs564536682	chr8:125627977-125627978	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs527326928	chr8:125627995-125627996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371672287	chr8:125628012-125628013	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs542098535	chr8:125628116-125628117	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs560597331	chr8:125628157-125628158	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs148569578	chr8:125628173-125628174	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs147060389	chr8:125628191-125628192	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs113524375	chr8:125628195-125628196	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535984435	chr8:125628236-125628237	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs3110541	chr8:125628285-125628286	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs549911842	chr8:125628293-125628294	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546031435	chr8:125628310-125628311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538923983	chr8:125628311-125628312	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558936407	chr8:125628320-125628321	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs72714747	chr8:125628336-125628337	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs16899858	chr8:125628342-125628343	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs554231900	chr8:125628358-125628359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141994885	chr8:125628376-125628377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542765133	chr8:125628404-125628405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs3110542	chr8:125628409-125628410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3110543	chr8:125628418-125628419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3110544	chr8:125628421-125628422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563052121	chr8:125628423-125628424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs3110545	chr8:125628430-125628431	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs545673591	chr8:125628438-125628439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78823505	chr8:125628472-125628473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11994513	chr8:125628486-125628487	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs546958177	chr8:125628539-125628540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375237895	chr8:125628542-125628543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114531105	chr8:125628556-125628557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs4871516	chr8:125628599-125628600	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs550737877	chr8:125628613-125628614	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs76723839	chr8:125628615-125628616	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs75442619	chr8:125628616-125628617	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs112058822	chr8:125628629-125628630	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs560138280	chr8:125628635-125628636	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs398009755	chr8:125628636-125628637	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs569826664	chr8:125628647-125628648	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs141833533	chr8:125628666-125628667	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs11994520	chr8:125628685-125628686	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs76300961	chr8:125628686-125628687	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs565953698	chr8:125628693-125628694	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs34038975	chr8:125628705-125628706	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs566610372	chr8:125628724-125628725	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs71576743	chr8:125628770-125628771	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:147)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Ovarian cancer	21240255	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3265 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125614000-125628800	Enhancers	Liver	Liver
2	chr8:125616000-125630200	Weak transcription	Rectal Smooth Muscle	rectum
3	chr8:125617600-125631400	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr8:125617800-125628600	Enhancers	Primary B cells from peripheral blood	blood
5	chr8:125618000-125632800	Weak transcription	HUVEC	blood vessel
6	chr8:125618000-125640400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr8:125619200-125630800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr8:125619200-125649000	Weak transcription	Colonic Mucosa	Colon
9	chr8:125619400-125628400	Weak transcription	Fetal Kidney	kidney
10	chr8:125621800-125631400	Weak transcription	Esophagus	oesophagus
11	chr8:125623200-125628400	Weak transcription	Fetal Lung	lung
12	chr8:125623200-125630800	Weak transcription	Pancreas	Pancrea
13	chr8:125623200-125631600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr8:125623400-125630800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr8:125623600-125630400	Weak transcription	Gastric	stomach
16	chr8:125624200-125633800	Enhancers	Brain Hippocampus Middle	brain
17	chr8:125624600-125629000	Weak transcription	HSMMtube	muscle
18	chr8:125624800-125628800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr8:125624800-125631200	Enhancers	Brain Germinal Matrix	brain
20	chr8:125624800-125633000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:125625000-125628200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:125625000-125628200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr8:125625000-125628600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr8:125625000-125629400	Weak transcription	Fetal Brain Male	brain
25	chr8:125625200-125634400	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr8:125625400-125628200	Weak transcription	Right Ventricle	heart
27	chr8:125625400-125630600	Enhancers	Primary B cells from cord blood	blood
28	chr8:125625400-125632200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr8:125625800-125628600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr8:125626000-125630800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:125626200-125629400	Weak transcription	Psoas Muscle	Psoas
32	chr8:125626200-125629800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:125626200-125630400	Weak transcription	Osteobl	bone
34	chr8:125626400-125628200	Weak transcription	Fetal Intestine Small	intestine
35	chr8:125626400-125630600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr8:125626400-125630800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:125626400-125631400	Enhancers	Adipose Nuclei	Adipose
38	chr8:125626400-125631400	Weak transcription	NHEK	skin
39	chr8:125626400-125638800	Weak transcription	HMEC	breast
40	chr8:125626600-125628600	Enhancers	Spleen	Spleen
41	chr8:125626600-125630600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr8:125626600-125635600	Enhancers	Fetal Heart	heart
43	chr8:125626800-125628400	Enhancers	Fetal Brain Female	brain
44	chr8:125627000-125629800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr8:125627000-125633400	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr8:125627000-125633600	Enhancers	Brain Cingulate Gyrus	brain
47	chr8:125627200-125628400	Enhancers	Lung	lung
48	chr8:125627200-125631400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr8:125627200-125631600	Enhancers	HepG2	liver
50	chr8:125627200-125632800	Enhancers	Brain Inferior Temporal Lobe	brain

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