Variant report

Variant	nsv1059494
Chromosome Location	chr20:25377602-25441835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:994)
CpG islands
(count:1040)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:994 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25387822-25388496	HepG2	liver:	n/a	chr20:25388309-25388317
2	ARID3A	chr20:25379639-25380138	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:25379777-25380076	K562	blood:	n/a	n/a
4	ARID3A	chr20:25388096-25388261	K562	blood:	n/a	n/a
5	ATF1	chr20:25397252-25397513	K562	blood:	n/a	n/a
6	ATF2	chr20:25388112-25388527	GM12878	blood:	n/a	n/a
7	ATF2	chr20:25387954-25388507	GM12878	blood:	n/a	n/a
8	ATF3	chr20:25387974-25388532	A549	lung:	n/a	chr20:25388194-25388203
9	ATF3	chr20:25388032-25388664	A549	lung:	n/a	chr20:25388194-25388203
10	BATF	chr20:25399506-25399665	GM12878	blood:	n/a	chr20:25399587-25399598
11	BATF	chr20:25387943-25388438	GM12878	blood:	n/a	chr20:25388072-25388081
12	BCL3	chr20:25387957-25388925	A549	lung:	n/a	chr20:25388326-25388335
13	BCL3	chr20:25387945-25388694	A549	lung:	n/a	chr20:25388326-25388335
14	BCL3	chr20:25388706-25389225	GM12878	blood:	n/a	n/a
15	BCLAF1	chr20:25388018-25388559	GM12878	blood:	n/a	chr20:25388326-25388335
16	BHLHE40	chr20:25379784-25380071	GM12878	blood:	n/a	n/a
17	BHLHE40	chr20:25399551-25399751	GM12878	blood:	n/a	n/a
18	BHLHE40	chr20:25388127-25388443	K562	blood:	n/a	n/a
19	BRCA1	chr20:25388053-25388627	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr20:25388152-25388535	HepG2	liver:	n/a	n/a
21	CBX3	chr20:25383211-25383531	K562	blood:	n/a	n/a
22	CBX3	chr20:25387960-25388580	K562	blood:	n/a	n/a
23	CBX3	chr20:25383243-25383515	K562	blood:	n/a	n/a
24	CCNT2	chr20:25388137-25388602	K562	blood:	n/a	n/a
25	CEBPB	chr20:25403148-25403243	HepG2	liver:	n/a	chr20:25403177-25403188
26	CEBPB	chr20:25403054-25403274	IMR90	lung:	n/a	chr20:25403177-25403188
27	CEBPB	chr20:25407589-25407872	IMR90	lung:	n/a	n/a
28	CEBPB	chr20:25392100-25392118	IMR90	lung:	n/a	n/a
29	CEBPB	chr20:25392080-25392206	A549	lung:	n/a	n/a
30	CEBPB	chr20:25407590-25407908	A549	lung:	n/a	n/a
31	CEBPB	chr20:25388111-25388409	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr20:25392007-25392170	HepG2	liver:	n/a	n/a
33	CEBPB	chr20:25399161-25399349	MCF-7	breast:	n/a	n/a
34	CEBPB	chr20:25394364-25394498	A549	lung:	n/a	n/a
35	CEBPB	chr20:25407604-25407908	HepG2	liver:	n/a	n/a
36	CEBPD	chr20:25387973-25388659	HepG2	liver:	n/a	n/a
37	CEBPZ	chr20:25379503-25379899	HepG2	liver:	n/a	n/a
38	CHD1	chr20:25387971-25389454	H1-hESC	embryonic stem cell:	n/a	chr20:25388585-25388595
39	CHD2	chr20:25388068-25388542	K562	blood:	n/a	n/a
40	CHD2	chr20:25388030-25388465	GM12878	blood:	n/a	n/a
41	CHD2	chr20:25388029-25388603	Hela-S3	cervix:	n/a	chr20:25388585-25388595
42	CHD2	chr20:25387911-25388569	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr20:25388145-25388567	HepG2	liver:	n/a	n/a
44	CREB1	chr20:25388098-25388364	A549	lung:	n/a	n/a
45	CREB1	chr20:25388007-25388662	A549	lung:	n/a	n/a
46	CREB1	chr20:25387891-25388879	HepG2	liver:	n/a	n/a
47	CTBP2	chr20:25388063-25388600	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr20:25379900-25380050	HepG2	liver:	n/a	n/a
49	CTCF	chr20:25379920-25380070	HFF	foreskin:	n/a	n/a
50	CTCF	chr20:25379664-25380150	HepG2	liver:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25433878-25433928	A549	lung:	n/a
2	chr20:25388779-25388829	HIPEpiC	eye:	n/a
3	chr20:25427961-25428011	NHDF-neo	bronchial:	n/a
4	chr20:25433878-25433928	A549	lung:	n/a
5	chr20:25388779-25388829	HIPEpiC	eye:	n/a
6	chr20:25427961-25428011	NHDF-neo	bronchial:	n/a
7	chr20:25388289-25388339	AG09309	skin:	n/a
8	chr20:25382007-25382057	HIPEpiC	eye:	n/a
9	chr20:25388369-25388419	NT2-D1	testis:	n/a
10	chr20:25386216-25386266	IMR90	lung:	fetal
11	chr20:25433878-25433928	HNPCEpiC	eye:	n/a
12	chr20:25388287-25388337	RPTEC	kidney:	n/a
13	chr20:25388779-25388829	HRCEpiC	kidney:	n/a
14	chr20:25388641-25388691	HCF	heart:	n/a
15	chr20:25433878-25433928	SAEC	small airway:	n/a
16	chr20:25382007-25382057	HCT-116	colon:	n/a
17	chr20:25388779-25388829	NHDF-neo	bronchial:	n/a
18	chr20:25427961-25428011	NT2-D1	testis:	n/a
19	chr20:25388289-25388339	HEEpiC	esophagus:	n/a
20	chr20:25388278-25388328	PFSK-1	brain:	n/a
21	chr20:25388049-25388099	SK-N-SH	brain:	n/a
22	chr20:25382007-25382057	Jurkat	blood:	n/a
23	chr20:25388369-25388419	HUVEC	blood vessel:	n/a
24	chr20:25382007-25382057	T-47D	breast:	n/a
25	chr20:25386216-25386266	BJ	skin:	n/a
26	chr20:25388199-25388249	HRCEpiC	kidney:	n/a
27	chr20:25388289-25388339	SK-N-SH_RA	brain:	n/a
28	chr20:25381464-25381514	NT2-D1	testis:	n/a
29	chr20:25388353-25388403	GM06990	blood:	n/a
30	chr20:25387977-25388027	HepG2	liver:	n/a
31	chr20:25381464-25381514	BE2_C	brain:	n/a
32	chr20:25388289-25388339	AG10803	skin:	n/a
33	chr20:25388353-25388403	HRCEpiC	kidney:	n/a
34	chr20:25388779-25388829	CMK	blood:	n/a
35	chr20:25387977-25388027	SAEC	small airway:	n/a
36	chr20:25386216-25386266	AG04450	lung:	fetal
37	chr20:25388278-25388328	K562	blood:	n/a
38	chr20:25388199-25388249	AG04450	lung:	fetal
39	chr20:25387977-25388027	GM19239	blood:	n/a
40	chr20:25388278-25388328	HRPEpiC	eye:	n/a
41	chr20:25388641-25388691	MCF-7	breast:	n/a
42	chr20:25388089-25388139	NH-A	brain:	n/a
43	chr20:25388089-25388139	H1-hESC	embryonic stem cell:	embryo
44	chr20:25392112-25392162	NT2-D1	testis:	n/a
45	chr20:25388353-25388403	NH-A	brain:	n/a
46	chr20:25388049-25388099	HepG2	liver:	n/a
47	chr20:25382007-25382057	AG09309	skin:	n/a
48	chr20:25381464-25381514	PFSK-1	brain:	n/a
49	chr20:25388049-25388099	AG04449	skin:	fetal
50	chr20:25388289-25388339	LNCaP	prostate:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:25388341..25390169-chr20:25397510..25399863,2	MCF-7	breast:
2	chr14:64971494..64972452-chr20:25388243..25388799,2	Hela-S3	cervix:
3	chr20:24972013..24974485-chr20:25388171..25390084,2	MCF-7	breast:
4	chr20:25274762..25275867-chr20:25379505..25380419,5	K562	blood:
5	chr20:25273820..25275552-chr20:25407200..25409099,2	K562	blood:
6	chr20:25289881..25292169-chr20:25388744..25391503,2	MCF-7	breast:
7	chr20:25431598..25433481-chr20:25439717..25442541,2	MCF-7	breast:
8	chr20:25274540..25275681-chr20:25379513..25380502,6	MCF-7	breast:
9	chr20:25369990..25372746-chr20:25384220..25386698,2	K562	blood:
10	chr20:24973762..24975336-chr20:25378149..25379762,2	MCF-7	breast:
11	chr20:25318544..25319155-chr20:25379499..25380008,2	MCF-7	breast:
12	chr20:25393485..25396024-chr20:25399784..25401777,2	K562	blood:
13	chr20:25389767..25391883-chr20:25602900..25605790,2	K562	blood:
14	chr20:25369196..25373772-chr20:25386901..25390344,6	MCF-7	breast:
15	chr20:25385575..25388779-chr20:25393238..25395970,3	K562	blood:
16	chr20:25369869..25371629-chr20:25378705..25380608,2	MCF-7	breast:
17	chr20:25387920..25388819-chr7:6048429..6049127,2	NB4	blood:
18	chr20:25431598..25433481-chr20:25439717..25442541,2	MCF-7	breast:
19	chr20:25316896..25317861-chr20:25379425..25380434,7	MCF-7	breast:
20	chr20:25367909..25369647-chr20:25375596..25377784,2	MCF-7	breast:
21	chr20:25388650..25390177-chr20:25402470..25404637,3	MCF-7	breast:
22	chr20:25295465..25296133-chr20:25379463..25380411,3	MCF-7	breast:
23	chr20:25275140..25276137-chr20:25379287..25380023,3	MCF-7	breast:
24	chr20:25274830..25275740-chr20:25378372..25379283,2	MCF-7	breast:
25	chr20:25383291..25386205-chr20:25386365..25388737,3	MCF-7	breast:
26	chr20:25388650..25390177-chr20:25402470..25404637,3	MCF-7	breast:
27	chr20:25371197..25373203-chr20:25390563..25392100,2	K562	blood:
28	chr20:25388255..25390330-chr20:25390563..25393927,5	MCF-7	breast:
29	chr20:25370156..25372734-chr20:25387934..25390472,3	MCF-7	breast:
30	chr20:25397786..25400078-chr20:25402229..25405600,3	MCF-7	breast:
31	chr20:24973500..24975861-chr20:25384259..25387078,2	MCF-7	breast:
32	chr20:25385575..25388779-chr20:25393238..25395970,3	K562	blood:
33	chr20:25382269..25384430-chr20:25387630..25389811,2	K562	blood:
34	chr20:25377062..25378773-chr20:25386652..25389539,2	K562	blood:
35	chr20:25426609..25429585-chr20:25546782..25548440,2	MCF-7	breast:
36	chr20:25401571..25403410-chr20:25403637..25405682,2	K562	blood:
37	chr20:25371197..25373195-chr20:25390563..25393020,2	K562	blood:
38	chr20:25316916..25317821-chr20:25379512..25380380,4	MCF-7	breast:
39	chr20:25397786..25400078-chr20:25402229..25405600,3	MCF-7	breast:
40	chr20:25392116..25394910-chr20:25395209..25398004,3	K562	blood:
41	chr20:25387859..25390842-chr20:25397411..25399483,2	MCF-7	breast:
42	chr20:25401571..25403410-chr20:25403637..25405682,2	K562	blood:
43	chr20:25388660..25391384-chr20:25394035..25397022,4	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GINS1	hsa-miR-7-5p	chr20:25428910-25428929

Variant related genes	Relation type
NINL	TF binding region
GINS1	TF binding region
NINL	CpG island
GINS1	CpG island
ENSG00000089775	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000101474	chromatin interactions
ENSG00000213742	chromatin interactions
ENSG00000106305	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000101003	chromatin interactions
ENSG00000100997	chromatin interactions
ENSG00000122512	chromatin interactions

Extended variants
information (count: 2681 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2681 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529259977	chr20:25377606-25377607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549021700	chr20:25377607-25377608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2263204	chr20:25377688-25377689	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs6083836	chr20:25377694-25377695	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528602482	chr20:25377718-25377719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs145291553	chr20:25377764-25377765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571379923	chr20:25377772-25377773	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2387880	chr20:25377787-25377788	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs550614564	chr20:25377788-25377789	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs567228620	chr20:25377868-25377869	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557370511	chr20:25377873-25377874	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182767972	chr20:25377924-25377925	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572962045	chr20:25377930-25377931	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs188883846	chr20:25377931-25377932	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs193249163	chr20:25377942-25377943	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374764735	chr20:25377952-25377953	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs578123574	chr20:25377961-25377962	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544053981	chr20:25377965-25377966	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs184471313	chr20:25377972-25377973	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs574043037	chr20:25377979-25377980	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546066968	chr20:25377988-25377989	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188966562	chr20:25377989-25377990	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs563982723	chr20:25378062-25378063	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528542483	chr20:25378075-25378076	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551606002	chr20:25378143-25378144	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564990290	chr20:25378150-25378151	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191879422	chr20:25378162-25378163	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2387881	chr20:25378172-25378173	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs550802599	chr20:25378179-25378180	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs371768525	chr20:25378187-25378188	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374929770	chr20:25378188-25378189	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536587960	chr20:25378197-25378198	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546599307	chr20:25378209-25378210	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541028956	chr20:25378249-25378250	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147631054	chr20:25378287-25378288	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs540788961	chr20:25378305-25378306	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs6083838	chr20:25378318-25378319	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs6083839	chr20:25378335-25378336	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs558379313	chr20:25378404-25378405	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs529646187	chr20:25378411-25378412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs548511216	chr20:25378422-25378423	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557174721	chr20:25378423-25378424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147984883	chr20:25378447-25378448	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs573977893	chr20:25378455-25378456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs577560922	chr20:25378504-25378505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs374130010	chr20:25378519-25378520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs370701068	chr20:25378550-25378551	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs569828040	chr20:25378606-25378607	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573170506	chr20:25378732-25378733	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs545440866	chr20:25378740-25378741	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1561 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25372000-25378000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr20:25372000-25379000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:25372200-25379000	Weak transcription	Brain Angular Gyrus	brain
4	chr20:25372200-25379000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr20:25372200-25380800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr20:25372400-25377800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr20:25372400-25379000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr20:25372400-25379200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr20:25374800-25379400	Weak transcription	Hela-S3	cervix
10	chr20:25375000-25379200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr20:25375000-25379200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr20:25375200-25379200	Weak transcription	Brain Hippocampus Middle	brain
13	chr20:25375200-25379200	Weak transcription	Brain Substantia Nigra	brain
14	chr20:25375400-25379000	Weak transcription	Brain Anterior Caudate	brain
15	chr20:25375400-25379600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr20:25375800-25379200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr20:25376000-25379000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr20:25377000-25378000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr20:25377400-25377800	Enhancers	Colonic Mucosa	Colon
20	chr20:25377400-25377800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr20:25377600-25377800	Enhancers	Duodenum Mucosa	Duodenum
22	chr20:25377600-25377800	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr20:25377600-25379800	Enhancers	GM12878-XiMat	blood
24	chr20:25377600-25381600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr20:25377800-25378000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr20:25377800-25378000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
27	chr20:25377800-25378000	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr20:25377800-25378200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr20:25377800-25378200	Active TSS	Colonic Mucosa	Colon
30	chr20:25377800-25378200	Flanking Active TSS	Duodenum Mucosa	Duodenum
31	chr20:25377800-25378200	Enhancers	K562	blood
32	chr20:25377800-25378400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr20:25377800-25378400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr20:25377800-25378400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr20:25377800-25380000	Enhancers	Fetal Intestine Large	intestine
36	chr20:25377800-25380000	Enhancers	Placenta	Placenta
37	chr20:25377800-25380200	Enhancers	Fetal Intestine Small	intestine
38	chr20:25378000-25378400	Active TSS	Rectal Mucosa Donor 29	rectum
39	chr20:25378000-25378600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr20:25378000-25379600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr20:25378000-25380000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr20:25378000-25380200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr20:25378000-25380400	Enhancers	A549	lung
44	chr20:25378200-25379400	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr20:25378200-25379400	Weak transcription	K562	blood
46	chr20:25378200-25379600	Enhancers	HepG2	liver
47	chr20:25378200-25379800	Enhancers	Duodenum Mucosa	Duodenum
48	chr20:25378200-25379800	Enhancers	NHLF	lung
49	chr20:25378400-25378800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr20:25378400-25379000	Enhancers	Rectal Mucosa Donor 29	rectum

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