Variant report

Variant	nsv548577
Chromosome Location	chr1:191195800-191721463
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1610)
CpG islands
(count:244)
Chromatin interactive
region (count:130)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:191338195-191338459	K562	blood:	n/a	n/a
2	ARID3A	chr1:191551379-191551439	K562	blood:	n/a	n/a
3	ARID3A	chr1:191467411-191467729	K562	blood:	n/a	n/a
4	ARID3A	chr1:191610568-191610666	K562	blood:	n/a	n/a
5	ARID3A	chr1:191618421-191618423	K562	blood:	n/a	n/a
6	ATF1	chr1:191515516-191515563	K562	blood:	n/a	n/a
7	ATF1	chr1:191297314-191297326	K562	blood:	n/a	n/a
8	ATF1	chr1:191567842-191568015	K562	blood:	n/a	n/a
9	ATF1	chr1:191398326-191398421	K562	blood:	n/a	n/a
10	ATF1	chr1:191576763-191576777	K562	blood:	n/a	n/a
11	ATF1	chr1:191338119-191338421	K562	blood:	n/a	n/a
12	ATF1	chr1:191433147-191433178	K562	blood:	n/a	n/a
13	ATF1	chr1:191637265-191637387	K562	blood:	n/a	n/a
14	ATF1	chr1:191551254-191551663	K562	blood:	n/a	n/a
15	ATF2	chr1:191551244-191551670	GM12878	blood:	n/a	n/a
16	ATF2	chr1:191551238-191551606	GM12878	blood:	n/a	n/a
17	ATF3	chr1:191373403-191373752	K562	blood:	n/a	n/a
18	BACH1	chr1:191587736-191587795	K562	blood:	n/a	n/a
19	BACH1	chr1:191671293-191671597	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr1:191460518-191460521	K562	blood:	n/a	n/a
21	BACH1	chr1:191671302-191671575	K562	blood:	n/a	n/a
22	BACH1	chr1:191274761-191274805	K562	blood:	n/a	n/a
23	BACH1	chr1:191253401-191253595	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:191389471-191389476	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr1:191668480-191668735	GM12878	blood:	n/a	chr1:191668644-191668655
26	BHLHE40	chr1:191338189-191338354	K562	blood:	n/a	n/a
27	BHLHE40	chr1:191259569-191259784	K562	blood:	n/a	n/a
28	BHLHE40	chr1:191551353-191551397	K562	blood:	n/a	n/a
29	BRCA1	chr1:191370538-191370577	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr1:191275577-191275852	K562	blood:	n/a	n/a
31	CBX3	chr1:191441528-191441847	K562	blood:	n/a	n/a
32	CBX3	chr1:191253318-191253712	K562	blood:	n/a	n/a
33	CBX3	chr1:191482212-191482596	K562	blood:	n/a	n/a
34	CBX3	chr1:191357458-191357801	K562	blood:	n/a	n/a
35	CBX3	chr1:191662926-191663304	K562	blood:	n/a	n/a
36	CBX3	chr1:191365747-191366197	K562	blood:	n/a	n/a
37	CBX3	chr1:191357460-191357656	K562	blood:	n/a	n/a
38	CBX3	chr1:191547951-191548371	K562	blood:	n/a	n/a
39	CBX3	chr1:191506193-191506517	K562	blood:	n/a	n/a
40	CBX3	chr1:191373433-191373795	K562	blood:	n/a	n/a
41	CBX3	chr1:191253357-191253679	K562	blood:	n/a	n/a
42	CBX3	chr1:191367627-191368055	K562	blood:	n/a	n/a
43	CBX3	chr1:191365898-191366123	K562	blood:	n/a	n/a
44	CBX3	chr1:191297007-191297287	K562	blood:	n/a	n/a
45	CBX3	chr1:191458327-191458683	K562	blood:	n/a	n/a
46	CBX3	chr1:191506145-191506554	K562	blood:	n/a	n/a
47	CBX3	chr1:191577454-191577763	K562	blood:	n/a	n/a
48	CCNT2	chr1:191353485-191353497	K562	blood:	n/a	n/a
49	CCNT2	chr1:191551290-191551637	K562	blood:	n/a	n/a
50	CCNT2	chr1:191544407-191544721	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:191503762-191503812	NHBE	bronchial:	n/a
2	chr1:191701857-191701907	Hela-S3	cervix:	n/a
3	chr1:191503762-191503812	BE2_C	brain:	n/a
4	chr1:191701782-191701832	HMEC	breast:	n/a
5	chr1:191503762-191503812	HCT-116	colon:	n/a
6	chr1:191701782-191701832	NHBE	bronchial:	n/a
7	chr1:191701782-191701832	Hepatocyte	liver:	n/a
8	chr1:191701782-191701832	ovcar-3	ovarian:	n/a
9	chr1:191701209-191701259	HEK293	kidney:	embryo
10	chr1:191503762-191503812	Hepatocyte	liver:	n/a
11	chr1:191701857-191701907	MCF-7	breast:	n/a
12	chr1:191701857-191701907	U87	brain:	n/a
13	chr1:191701782-191701832	HRE	kidney:	n/a
14	chr1:191503762-191503812	GM12892	blood:	n/a
15	chr1:191503762-191503812	Caco-2	colon:	n/a
16	chr1:191701209-191701259	SAEC	small airway:	n/a
17	chr1:191701209-191701259	NH-A	brain:	n/a
18	chr1:191701209-191701259	ProgFib	skin:	n/a
19	chr1:191701209-191701259	AG04449	skin:	fetal
20	chr1:191503762-191503812	CMK	blood:	n/a
21	chr1:191503762-191503812	HCM	heart:	n/a
22	chr1:191701782-191701832	AG04449	skin:	fetal
23	chr1:191701782-191701832	Jurkat	blood:	n/a
24	chr1:191503762-191503812	Hela-S3	cervix:	n/a
25	chr1:191701857-191701907	HIPEpiC	eye:	n/a
26	chr1:191701209-191701259	RPTEC	kidney:	n/a
27	chr1:191503762-191503812	K562	blood:	n/a
28	chr1:191701782-191701832	GM12878	blood:	n/a
29	chr1:191701782-191701832	ProgFib	skin:	n/a
30	chr1:191503762-191503812	AG09309	skin:	n/a
31	chr1:191701209-191701259	T-47D	breast:	n/a
32	chr1:191701209-191701259	K562	blood:	n/a
33	chr1:191503762-191503812	MCF10A-Er-Src	breast:	n/a
34	chr1:191503762-191503812	GM06990	blood:	n/a
35	chr1:191701782-191701832	SK-N-MC	brain:	n/a
36	chr1:191701209-191701259	HL-60	blood:	n/a
37	chr1:191701209-191701259	PANC-1	pancreas:	n/a
38	chr1:191701782-191701832	PrEC	prostate:	n/a
39	chr1:191701857-191701907	HCT-116	colon:	n/a
40	chr1:191701857-191701907	Jurkat	blood:	n/a
41	chr1:191701782-191701832	HAEpiC	amniotic membrane:	n/a
42	chr1:191503762-191503812	A549	lung:	n/a
43	chr1:191701782-191701832	HEEpiC	esophagus:	n/a
44	chr1:191503762-191503812	HepG2	liver:	n/a
45	chr1:191701209-191701259	HRPEpiC	eye:	n/a
46	chr1:191701857-191701907	RPTEC	kidney:	n/a
47	chr1:191701782-191701832	PANC-1	pancreas:	n/a
48	chr1:191701857-191701907	HUVEC	blood vessel:	n/a
49	chr1:191503762-191503812	HRCEpiC	kidney:	n/a
50	chr1:191701782-191701832	AG04450	lung:	fetal

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:191531038..191532932-chr1:191533224..191534815,2	MCF-7	breast:
2	chr1:191704245..191706560-chr1:191706732..191709677,2	K562	blood:
3	chr1:191473798..191475673-chr1:191477416..191479078,2	K562	blood:
4	chr1:191580900..191582708-chr1:191592956..191594970,2	K562	blood:
5	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
6	chr1:191592940..191595945-chr1:191597443..191599181,3	K562	blood:
7	chr1:191605237..191607003-chr1:191610030..191611864,2	K562	blood:
8	chr1:191711996..191714385-chr1:191821887..191824152,2	K562	blood:
9	chr1:191368248..191370695-chr1:191372787..191374561,2	K562	blood:
10	chr1:191502483..191504253-chr17:56707440..56709288,2	MCF-7	breast:
11	chr1:191287950..191289463-chr1:191291967..191294234,2	K562	blood:
12	chr1:191311585..191313743-chr1:191315163..191316847,2	K562	blood:
13	chr1:191666098..191668261-chr1:191671112..191673140,2	MCF-7	breast:
14	chr1:191611871..191613494-chr1:191619037..191620798,2	K562	blood:
15	chr1:191501593..191503372-chr1:191505633..191507558,2	K562	blood:
16	chr1:191708525..191710416-chr1:191713003..191715158,2	K562	blood:
17	chr1:191618527..191620299-chr1:191625178..191627507,2	K562	blood:
18	chr1:191285545..191288478-chr1:191311947..191313590,2	MCF-7	breast:
19	chr1:191277227..191279088-chr1:191280511..191283131,2	K562	blood:
20	chr1:191401913..191403539-chr1:191421067..191423069,2	K562	blood:
21	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
22	chr1:191446579..191448734-chr1:191448967..191451024,2	MCF-7	breast:
23	chr1:191450148..191453626-chr1:191453943..191457136,3	K562	blood:
24	chr1:191371943..191373778-chr1:191427254..191429182,2	K562	blood:
25	chr1:191611871..191613494-chr1:191619037..191620798,2	K562	blood:
26	chr1:191476619..191478729-chr1:191489630..191491476,2	K562	blood:
27	chr1:191235053..191236832-chr1:191299467..191301857,2	MCF-7	breast:
28	chr1:191426971..191427787-chr8:122736326..122736882,2	MCF-7	breast:
29	chr1:191424584..191426458-chr1:191426540..191428604,2	MCF-7	breast:
30	chr1:191212442..191214167-chr1:191217333..191219833,2	MCF-7	breast:
31	chr1:191532249..191535067-chr1:191535515..191537308,2	K562	blood:
32	chr1:191719906..191721818-chr1:191723940..191725758,2	K562	blood:
33	chr1:191580900..191582708-chr1:191592956..191594970,2	K562	blood:
34	chr1:191251451..191253394-chr1:191255335..191256855,2	K562	blood:
35	chr1:191433727..191435829-chr1:191471858..191473427,2	K562	blood:
36	chr1:191389236..191391019-chr1:191392844..191394511,2	K562	blood:
37	chr1:191455290..191457922-chr1:191460809..191463001,2	MCF-7	breast:
38	chr1:191424584..191426458-chr1:191426540..191428604,2	MCF-7	breast:
39	chr1:191701608..191705437-chr1:191706302..191708932,3	K562	blood:
40	chr1:191420711..191422302-chr1:191475055..191477121,2	K562	blood:
41	chr1:191367727..191369748-chr1:191373061..191374879,2	K562	blood:
42	chr1:191262328..191265076-chr1:191299134..191300928,2	K562	blood:
43	chr1:191531038..191532932-chr1:191533224..191534815,2	MCF-7	breast:
44	chr1:191421290..191423528-chr1:191424366..191426251,2	K562	blood:
45	chr1:191287950..191289463-chr1:191291967..191294234,2	K562	blood:
46	chr1:76262387..76264305-chr1:191498781..191500281,2	K562	blood:
47	chr1:191590246..191592649-chr1:191593874..191595968,2	MCF-7	breast:
48	chr1:191250975..191253394-chr1:191254576..191256855,3	K562	blood:
49	chr1:191605237..191607003-chr1:191610030..191611864,2	K562	blood:
50	chr1:191446579..191448734-chr1:191448967..191451024,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-9	chr1:191601401-191601706	NONHSAT008519
2	lnc-FAM5C-3	chr1:191685359-191685577	XLOC_001131
3	lnc-RGS18-10	chr1:191494155-191494355	expReg_chr1_21196_+
4	lnc-RGS18-9	chr1:191586857-191586992	NONHSAT008519
5	lnc-FAM5C-3	chr1:191686588-191686611	XLOC_001131
6	lnc-RGS18-9	chr1:191540498-191540691	NONHSAT008519
7	lnc-RGS18-2	chr1:191197453-191197597	XLOC_000506
8	lnc-FAM5C-13	chr1:191487184-191487423	predAs_chen_BG220711_1
9	lnc-RGS18-9	chr1:191584886-191585028	NONHSAT008519
10	lnc-FAM5C-12	chr1:191197453-191197597	ENSG00000233882.2

No data

Variant related genes	Relation type
ENSG00000233882	TF binding region
ENSG00000233882	CpG island
ENSG00000212195	chromatin interactions
ENSG00000271187	chromatin interactions
ENSG00000057468	chromatin interactions
GSK3B	miRNA target sites
G6PC3	miRNA target sites
ARSB	miRNA target sites

Extended variants
information (count: 6269 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:6269 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7418163	chr1:191195800-191195801	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531461315	chr1:191197473-191197474	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs530996949	chr1:191197517-191197518	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs140037125	chr1:191199816-191199817	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs546205813	chr1:191199853-191199854	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs563216583	chr1:191199856-191199857	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs6660971	chr1:191199876-191199877	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs558324016	chr1:191202523-191202524	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs74323479	chr1:191209638-191209639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs193209755	chr1:191209710-191209711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559885960	chr1:191209720-191209721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528814995	chr1:191209748-191209749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551633348	chr1:191209749-191209750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565207314	chr1:191209776-191209777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573403797	chr1:191210476-191210477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74130109	chr1:191210529-191210530	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs565245795	chr1:191210571-191210572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540466238	chr1:191224402-191224403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77123358	chr1:191224423-191224424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376251363	chr1:191224442-191224443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188453955	chr1:191224468-191224469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552201781	chr1:191224533-191224534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192537578	chr1:191224547-191224548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530817824	chr1:191224557-191224558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563050761	chr1:191224583-191224584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531091380	chr1:191224601-191224602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs367602315	chr1:191224602-191224603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567463984	chr1:191224622-191224623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536332514	chr1:191224653-191224654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs146398361	chr1:191224744-191224745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185332736	chr1:191224751-191224752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566973940	chr1:191224755-191224756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs539188428	chr1:191224778-191224779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111251051	chr1:191224781-191224782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147731798	chr1:191224782-191224783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs5779567	chr1:191224784-191224785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs3035697	chr1:191224785-191224786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34209644	chr1:191224786-191224787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs61053547	chr1:191224787-191224788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139657160	chr1:191224815-191224816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1454346	chr1:191224832-191224833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs370325532	chr1:191224871-191224872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188814018	chr1:191224882-191224883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192602014	chr1:191224900-191224901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184806785	chr1:191224936-191224937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs1246824	chr1:191224970-191224971	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs553866494	chr1:191224998-191224999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs189256254	chr1:191225004-191225005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181042504	chr1:191225020-191225021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376613504	chr1:191225024-191225025	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Lung adenocarcinoma	21935476	CNVD
Glioblastoma multiforme	21510904	CNVD
Intellectual disability	21811512	CNVD
Parathyroid adenoma	20824076	CNVD

Chromatin state (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:191194600-191195800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:191209600-191209800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr1:191210400-191210600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:191224400-191225200	Enhancers	Dnd41	blood
5	chr1:191224400-191225800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:191224400-191225800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:191228600-191230800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:191228800-191230800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:191229200-191230600	Enhancers	Primary hematopoietic stem cells	blood
10	chr1:191229600-191230400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr1:191230200-191230400	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr1:191244600-191244800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:191250400-191253600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:191252000-191252200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr1:191258800-191259800	Enhancers	Fetal Kidney	kidney
16	chr1:191259400-191260000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr1:191259400-191260000	Enhancers	Fetal Brain Male	brain
18	chr1:191259600-191260000	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr1:191259600-191260200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:191259600-191260400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr1:191275800-191276400	ZNF genes & repeats	Dnd41	blood
22	chr1:191287000-191288000	Enhancers	Fetal Heart	heart
23	chr1:191289200-191289600	Enhancers	Dnd41	blood
24	chr1:191312600-191314000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:191312800-191313400	Enhancers	Placenta	Placenta
26	chr1:191312800-191313600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:191312800-191314000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:191320000-191320400	Enhancers	Esophagus	oesophagus
29	chr1:191334000-191334600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:191334200-191334600	Enhancers	K562	blood
31	chr1:191337800-191338600	Active TSS	Pancreas	Pancrea
32	chr1:191337800-191339600	Active TSS	K562	blood
33	chr1:191338000-191338200	Enhancers	Colon Smooth Muscle	Colon
34	chr1:191338000-191338600	Active TSS	Rectal Smooth Muscle	rectum
35	chr1:191338000-191339800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr1:191338200-191338400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr1:191338200-191338400	Enhancers	Stomach Smooth Muscle	stomach
38	chr1:191338200-191338800	Active TSS	A549	lung
39	chr1:191338200-191339000	Active TSS	Colon Smooth Muscle	Colon
40	chr1:191338200-191339400	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr1:191338200-191339600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr1:191338200-191339800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr1:191338400-191339200	Enhancers	H1 Cell Line	embryonic stem cell
44	chr1:191338400-191339400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr1:191338400-191340600	Weak transcription	Stomach Smooth Muscle	stomach
46	chr1:191338600-191339200	Weak transcription	Rectal Smooth Muscle	rectum
47	chr1:191338600-191339600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:191338600-191340800	Weak transcription	Pancreas	Pancrea
49	chr1:191339000-191339200	Flanking Active TSS	Colon Smooth Muscle	Colon
50	chr1:191339000-191339800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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