Variant report

Variant	nsv871172
Chromosome Location	chr1:94504545-94535546
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1590)
CpG islands
(count:368)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1590 , 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	chr1:94533701-94534898	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:94527001-94527344	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:94511076-94511450	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:94528881-94529252	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:94511138-94511577	K562	blood:	n/a	n/a
6	ARID3A	chr1:94527623-94527960	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:94509776-94510237	HepG2	liver:	n/a	n/a
8	ATF2	chr1:94511131-94511601	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr1:94511008-94511557	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr1:94511186-94511564	A549	lung:	n/a	chr1:94511395-94511415
11	ATF3	chr1:94511165-94511601	A549	lung:	n/a	chr1:94511395-94511415
12	ATF3	chr1:94511275-94511474	K562	blood:	n/a	chr1:94511395-94511415
13	BACH1	chr1:94511207-94511564	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCLAF1	chr1:94527017-94527373	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:94527098-94527320	K562	blood:	n/a	n/a
16	BHLHE40	chr1:94511159-94511584	K562	blood:	n/a	n/a
17	BHLHE40	chr1:94527094-94527326	GM12878	blood:	n/a	n/a
18	BHLHE40	chr1:94511150-94511537	HepG2	liver:	n/a	n/a
19	BHLHE40	chr1:94509789-94510667	HepG2	liver:	n/a	n/a
20	BRCA1	chr1:94527009-94527289	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr1:94527097-94527338	HepG2	liver:	n/a	n/a
22	BRCA1	chr1:94511073-94511423	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr1:94528983-94529075	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr1:94533607-94534251	HCT-116	colon:	n/a	n/a
25	CBX3	chr1:94533433-94534347	HCT-116	colon:	n/a	n/a
26	CEBPB	chr1:94533932-94534258	A549	lung:	n/a	n/a
27	CEBPB	chr1:94505069-94505389	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:94533513-94534292	HCT-116	colon:	n/a	chr1:94533522-94533533 chr1:94534248-94534261
29	CEBPB	chr1:94533842-94534042	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:94511286-94511570	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:94527607-94527954	IMR90	lung:	n/a	n/a
32	CEBPB	chr1:94505124-94505324	HepG2	liver:	n/a	n/a
33	CEBPB	chr1:94533394-94534173	ECC-1	luminal epithelium:	n/a	chr1:94533522-94533533
34	CEBPB	chr1:94529020-94529087	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:94527684-94527801	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr1:94533776-94534285	HepG2	liver:	n/a	chr1:94534248-94534261
37	CEBPB	chr1:94527586-94527971	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:94508026-94508181	A549	lung:	n/a	n/a
39	CEBPB	chr1:94527540-94527953	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:94507968-94508242	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr1:94527649-94527935	A549	lung:	n/a	n/a
42	CEBPB	chr1:94527634-94527873	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:94527581-94527977	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:94528769-94529093	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:94513992-94514301	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:94511016-94511497	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr1:94527621-94527898	MCF-7	breast:	n/a	n/a
48	CEBPB	chr1:94527649-94527834	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr1:94507933-94508276	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:94533752-94534155	Hela-S3	cervix:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94511426-94511476	HCM	heart:	n/a
2	chr1:94514548-94514598	Hepatocyte	liver:	n/a
3	chr1:94511426-94511476	HCM	heart:	n/a
4	chr1:94514548-94514598	Hepatocyte	liver:	n/a
5	chr1:94511426-94511476	Jurkat	blood:	n/a
6	chr1:94511166-94511216	HCF	heart:	n/a
7	chr1:94514548-94514598	HEEpiC	esophagus:	n/a
8	chr1:94528115-94528165	ECC-1	luminal epithelium:	n/a
9	chr1:94504969-94505019	ProgFib	skin:	n/a
10	chr1:94511426-94511476	HNPCEpiC	eye:	n/a
11	chr1:94511166-94511216	PFSK-1	brain:	n/a
12	chr1:94528115-94528165	GM06990	blood:	n/a
13	chr1:94511166-94511216	SKMC	muscle:	n/a
14	chr1:94514548-94514598	SKMC	muscle:	n/a
15	chr1:94511426-94511476	HCPEpiC	choroid plexus:	n/a
16	chr1:94511166-94511216	NHDF-neo	bronchial:	n/a
17	chr1:94514548-94514598	GM06990	blood:	n/a
18	chr1:94504969-94505019	HCPEpiC	choroid plexus:	n/a
19	chr1:94511166-94511216	T-47D	breast:	n/a
20	chr1:94534645-94534695	GM12892	blood:	n/a
21	chr1:94511426-94511476	K562	blood:	n/a
22	chr1:94534645-94534695	Caco-2	colon:	n/a
23	chr1:94511166-94511216	GM12891	blood:	n/a
24	chr1:94511166-94511216	HMEC	breast:	n/a
25	chr1:94528115-94528165	AG09319	gingival:	n/a
26	chr1:94511426-94511476	ovcar-3	ovarian:	n/a
27	chr1:94514548-94514598	NT2-D1	testis:	n/a
28	chr1:94528115-94528165	HEEpiC	esophagus:	n/a
29	chr1:94511166-94511216	SAEC	small airway:	n/a
30	chr1:94514548-94514598	NHBE	bronchial:	n/a
31	chr1:94534645-94534695	HEEpiC	esophagus:	n/a
32	chr1:94504969-94505019	SAEC	small airway:	n/a
33	chr1:94511166-94511216	HepG2	liver:	n/a
34	chr1:94511166-94511216	IMR90	lung:	fetal
35	chr1:94504969-94505019	SK-N-SH_RA	brain:	n/a
36	chr1:94534645-94534695	SAEC	small airway:	n/a
37	chr1:94514548-94514598	T-47D	breast:	n/a
38	chr1:94511166-94511216	K562	blood:	n/a
39	chr1:94528115-94528165	HAEpiC	amniotic membrane:	n/a
40	chr1:94514548-94514598	K562	blood:	n/a
41	chr1:94534645-94534695	HCF	heart:	n/a
42	chr1:94534645-94534695	MCF10A-Er-Src	breast:	n/a
43	chr1:94504969-94505019	HEEpiC	esophagus:	n/a
44	chr1:94511166-94511216	Hepatocyte	liver:	n/a
45	chr1:94534645-94534695	HCT-116	colon:	n/a
46	chr1:94511426-94511476	HRCEpiC	kidney:	n/a
47	chr1:94534645-94534695	HCPEpiC	choroid plexus:	n/a
48	chr1:94534645-94534695	HRCEpiC	kidney:	n/a
49	chr1:94514548-94514598	BE2_C	brain:	n/a
50	chr1:94511426-94511476	AG09309	skin:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:94532845..94535328-chr1:94609574..94612339,2	MCF-7	breast:
2	chr1:94373717..94376146-chr1:94504477..94506025,2	MCF-7	breast:
3	chr1:94491175..94491813-chr1:94510908..94511574,2	MCF-7	breast:
4	chr1:94505445..94507921-chr1:94508358..94510832,2	K562	blood:
5	chr1:94529817..94533865-chr1:94534670..94536843,3	MCF-7	breast:
6	chr1:94528993..94529506-chr1:94706216..94707195,2	MCF-7	breast:
7	chr1:94502330..94505107-chr1:94527585..94529424,2	MCF-7	breast:
8	chr1:94529817..94533865-chr1:94534670..94536843,3	MCF-7	breast:
9	chr1:94526671..94528632-chr1:94533088..94535694,2	K562	blood:
10	chr1:94524835..94527724-chr1:94798552..94800345,2	MCF-7	breast:
11	chr1:94505022..94505841-chr1:94801175..94801955,3	K562	blood:
12	chr1:94505445..94507921-chr1:94508358..94510832,2	K562	blood:
13	chr1:94510338..94511868-chr1:94800755..94802089,7	MCF-7	breast:
14	chr1:94532482..94534156-chr1:94582374..94584202,2	MCF-7	breast:
15	chr1:94527285..94528858-chr1:94532743..94535509,2	MCF-7	breast:
16	chr1:94491226..94491950-chr1:94505185..94505725,2	MCF-7	breast:
17	chr1:94517264..94519171-chr1:94520165..94522225,2	K562	blood:
18	chr1:94527081..94529532-chr1:94702506..94704195,2	MCF-7	breast:
19	chr1:94504792..94505809-chr1:94801226..94802348,4	MCF-7	breast:
20	chr1:94528533..94530442-chr1:94567755..94569846,3	MCF-7	breast:
21	chr1:94527064..94527740-chr1:94706101..94706691,3	MCF-7	breast:
22	chr1:94527833..94529893-chr1:94702894..94705764,2	MCF-7	breast:
23	chr1:94502816..94505360-chr1:94694750..94697690,2	MCF-7	breast:
24	chr1:94509075..94510685-chr1:94516003..94517889,2	MCF-7	breast:
25	chr1:94509075..94510685-chr1:94516003..94517889,2	MCF-7	breast:
26	chr1:94504965..94505747-chr1:94801282..94802123,3	MCF-7	breast:
27	chr1:94510948..94511922-chr1:94929239..94929819,2	K562	blood:
28	chr1:94522843..94524816-chr1:94526964..94529105,2	K562	blood:
29	chr1:94532251..94537168-chr1:94582958..94586481,4	MCF-7	breast:
30	chr1:94526735..94527649-chr1:94702636..94703585,3	MCF-7	breast:
31	chr1:94533904..94535691-chr1:94564792..94567232,2	MCF-7	breast:
32	chr1:94532586..94535624-chr1:94566931..94569461,4	MCF-7	breast:
33	chr1:94517264..94519171-chr1:94520165..94522225,2	K562	blood:
34	chr1:94527285..94528858-chr1:94532743..94535509,2	MCF-7	breast:
35	chr1:94502330..94505107-chr1:94527585..94529424,2	MCF-7	breast:

No data

Variant related genes	Relation type
ABCA4	TF binding region
ABCA4	CpG island
ENSG00000226835	chromatin interactions
ENSG00000023909	chromatin interactions
ENSG00000233482	chromatin interactions
ENSG00000198691	chromatin interactions
ENSG00000137962	chromatin interactions

Extended variants
information (count: 1415 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11165069	chr1:94504545-94504546	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549411540	chr1:94504555-94504556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs185202361	chr1:94504578-94504579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs575189227	chr1:94504685-94504686	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs187490202	chr1:94504730-94504731	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191638857	chr1:94504746-94504747	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572995436	chr1:94504760-94504761	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530504585	chr1:94504761-94504762	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs561834883	chr1:94504799-94504800	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372540517	chr1:94504812-94504813	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184148275	chr1:94504828-94504829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141767708	chr1:94504833-94504834	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150594265	chr1:94504841-94504842	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371066777	chr1:94504875-94504876	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570501179	chr1:94504919-94504920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs372494832	chr1:94505009-94505010	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs571017359	chr1:94505057-94505058	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139543506	chr1:94505059-94505060	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs34119624	chr1:94505086-94505087	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs376268785	chr1:94505087-94505088	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534982946	chr1:94505112-94505113	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs568570066	chr1:94505154-94505155	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567482611	chr1:94505198-94505199	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs374800331	chr1:94505226-94505227	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs372791967	chr1:94505236-94505237	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs114658756	chr1:94505275-94505276	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs575230984	chr1:94505290-94505291	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539401648	chr1:94505340-94505341	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs558039116	chr1:94505349-94505350	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs573016550	chr1:94505350-94505351	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs540442355	chr1:94505481-94505482	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs281865390	chr1:94505567-94505568	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371375477	chr1:94505573-94505574	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374630957	chr1:94505586-94505587	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs61752421	chr1:94505598-94505599	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs368951547	chr1:94505603-94505604	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs61750126	chr1:94505604-94505605	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs137853898	chr1:94505611-94505612	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370967816	chr1:94505620-94505621	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs149503495	chr1:94505621-94505622	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs374610040	chr1:94505627-94505628	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187965758	chr1:94505630-94505631	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368692594	chr1:94505638-94505639	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370644803	chr1:94505643-94505644	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs138761163	chr1:94505645-94505646	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs387906388	chr1:94505652-94505653	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs75267647	chr1:94505659-94505660	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs267598773	chr1:94505667-94505668	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs61750125	chr1:94505675-94505676	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs62645954	chr1:94505678-94505679	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1106 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94488200-94505000	Weak transcription	Spleen	Spleen
2	chr1:94492200-94510000	Weak transcription	Aorta	Aorta
3	chr1:94496800-94508400	Weak transcription	Gastric	stomach
4	chr1:94497200-94505000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:94497400-94505000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:94497600-94505000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:94497600-94505200	Weak transcription	Lung	lung
8	chr1:94501200-94506000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:94501400-94505200	Enhancers	Hela-S3	cervix
10	chr1:94501800-94510000	Weak transcription	Pancreas	Pancrea
11	chr1:94502000-94505800	Enhancers	Osteobl	bone
12	chr1:94502000-94506000	Enhancers	Placenta Amnion	Placenta Amnion
13	chr1:94502000-94506800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr1:94502600-94505200	Enhancers	HSMMtube	muscle
15	chr1:94502600-94505600	Enhancers	HMEC	breast
16	chr1:94502600-94505800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr1:94502800-94507000	Enhancers	Fetal Muscle Leg	muscle
18	chr1:94503200-94506400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr1:94503400-94505000	Weak transcription	Fetal Muscle Trunk	muscle
20	chr1:94503400-94505000	Weak transcription	A549	lung
21	chr1:94503600-94505200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:94503800-94504600	Weak transcription	Left Ventricle	heart
23	chr1:94503800-94505000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr1:94503800-94505000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:94503800-94505000	Weak transcription	Right Atrium	heart
26	chr1:94503800-94505000	Weak transcription	HepG2	liver
27	chr1:94503800-94505200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:94503800-94505200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr1:94503800-94505400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:94503800-94510200	Weak transcription	Ovary	ovary
31	chr1:94504000-94505000	Weak transcription	NHEK	skin
32	chr1:94504000-94505200	Enhancers	HSMM	muscle
33	chr1:94504000-94505400	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr1:94504000-94505600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr1:94504000-94505600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:94504000-94506200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:94504000-94506600	Enhancers	HUVEC	blood vessel
38	chr1:94504200-94505600	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr1:94504200-94505800	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr1:94504200-94506000	Enhancers	NH-A	brain
41	chr1:94504200-94506400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:94504400-94504800	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr1:94504400-94505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr1:94504400-94505400	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr1:94504600-94504800	Enhancers	Colonic Mucosa	Colon
46	chr1:94504600-94504800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
47	chr1:94504600-94505400	Weak transcription	Fetal Stomach	stomach
48	chr1:94504600-94505800	Enhancers	Adipose Nuclei	Adipose
49	chr1:94504600-94506000	Enhancers	Left Ventricle	heart
50	chr1:94504800-94505600	Enhancers	HUES6 Cell Line	embryonic stem cell

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