Variant report

Variant	nsv599118
Chromosome Location	chr5:98358191-99029453
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2232)
CpG islands
(count:550)
Chromatin interactive
region (count:106)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2232 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:98440177-98440554	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:98440171-98440602	K562	blood:	n/a	n/a
3	ARID3A	chr5:98368173-98368614	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:98396074-98396378	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:98412592-98412893	K562	blood:	n/a	n/a
6	ARID3A	chr5:98396056-98396390	K562	blood:	n/a	n/a
7	ARID3A	chr5:98513499-98513769	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:98384349-98384443	K562	blood:	n/a	n/a
9	ARID3A	chr5:98360857-98361465	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:98368054-98368631	K562	blood:	n/a	n/a
11	ATF1	chr5:98382137-98382256	K562	blood:	n/a	n/a
12	ATF1	chr5:98368004-98368673	K562	blood:	n/a	n/a
13	ATF2	chr5:98404595-98405040	GM12878	blood:	n/a	n/a
14	ATF2	chr5:98395329-98395786	GM12878	blood:	n/a	n/a
15	ATF2	chr5:98362836-98363786	GM12878	blood:	n/a	n/a
16	ATF2	chr5:98362789-98363726	GM12878	blood:	n/a	n/a
17	ATF3	chr5:98440190-98440499	K562	blood:	n/a	n/a
18	BACH1	chr5:98512372-98512412	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:98582430-98582493	K562	blood:	n/a	n/a
20	BACH1	chr5:98630961-98630981	K562	blood:	n/a	n/a
21	BACH1	chr5:98477485-98477618	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr5:98752315-98752536	GM12878	blood:	n/a	n/a
23	BATF	chr5:98864846-98865096	GM12878	blood:	n/a	n/a
24	BATF	chr5:98362962-98363571	GM12878	blood:	n/a	n/a
25	BATF	chr5:98814204-98814519	GM12878	blood:	n/a	n/a
26	BATF	chr5:98362906-98363586	GM12878	blood:	n/a	n/a
27	BATF	chr5:98752295-98752532	GM12878	blood:	n/a	n/a
28	BATF	chr5:98814202-98814524	GM12878	blood:	n/a	n/a
29	BCL11A	chr5:98362936-98363611	GM12878	blood:	n/a	n/a
30	BCL11A	chr5:98814165-98814533	GM12878	blood:	n/a	n/a
31	BCL11A	chr5:98362950-98363600	GM12878	blood:	n/a	n/a
32	BCL3	chr5:98567093-98567361	GM12878	blood:	n/a	n/a
33	BCL3	chr5:98362923-98363619	GM12878	blood:	n/a	n/a
34	BCLAF1	chr5:98362804-98363631	GM12878	blood:	n/a	n/a
35	BCLAF1	chr5:98362899-98363602	GM12878	blood:	n/a	n/a
36	BHLHE40	chr5:98362911-98363866	GM12878	blood:	n/a	n/a
37	BHLHE40	chr5:98364085-98364812	GM12878	blood:	n/a	n/a
38	BHLHE40	chr5:98430943-98431038	K562	blood:	n/a	n/a
39	BHLHE40	chr5:98373578-98373606	HepG2	liver:	n/a	n/a
40	BHLHE40	chr5:98395388-98395751	GM12878	blood:	n/a	n/a
41	BHLHE40	chr5:98390879-98390930	GM12878	blood:	n/a	n/a
42	BRCA1	chr5:98472814-98472893	GM12878	blood:	n/a	n/a
43	BRCA1	chr5:98396066-98396439	H1-hESC	embryonic stem cell:	n/a	n/a
44	CBX3	chr5:98862548-98862851	K562	blood:	n/a	n/a
45	CBX3	chr5:98357819-98358338	K562	blood:	n/a	n/a
46	CBX3	chr5:98368120-98368708	K562	blood:	n/a	n/a
47	CCNT2	chr5:98368106-98368633	K562	blood:	n/a	n/a
48	CCNT2	chr5:98927320-98927465	K562	blood:	n/a	n/a
49	CCNT2	chr5:98402732-98402890	K562	blood:	n/a	n/a
50	CEBPB	chr5:98942379-98942440	HepG2	liver:	n/a	chr5:98942416-98942427

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:98860157-98860207	HCF	heart:	n/a
2	chr5:98860157-98860207	HCF	heart:	n/a
3	chr5:98396620-98396670	AG10803	skin:	n/a
4	chr5:98860157-98860207	MCF10A-Er-Src	breast:	n/a
5	chr5:98396620-98396670	GM06990	blood:	n/a
6	chr5:98746281-98746331	AG09319	gingival:	n/a
7	chr5:98541783-98541833	LNCaP	prostate:	n/a
8	chr5:98541824-98541874	GM06990	blood:	n/a
9	chr5:98368443-98368493	MCF-7	breast:	n/a
10	chr5:98541783-98541833	GM12892	blood:	n/a
11	chr5:98541783-98541833	AG09319	gingival:	n/a
12	chr5:98714340-98714390	HCF	heart:	n/a
13	chr5:98541874-98541924	GM06990	blood:	n/a
14	chr5:98541783-98541833	HIPEpiC	eye:	n/a
15	chr5:98541824-98541874	NHDF-neo	bronchial:	n/a
16	chr5:98541824-98541874	PANC-1	pancreas:	n/a
17	chr5:98396620-98396670	AG04449	skin:	fetal
18	chr5:98714340-98714390	GM12878	blood:	n/a
19	chr5:98368443-98368493	BE2_C	brain:	n/a
20	chr5:98541824-98541874	NB4	blood:	n/a
21	chr5:98541783-98541833	Hepatocyte	liver:	n/a
22	chr5:98368443-98368493	SK-N-MC	brain:	n/a
23	chr5:98368443-98368493	HEK293	kidney:	embryo
24	chr5:98714340-98714390	AG09319	gingival:	n/a
25	chr5:98541874-98541924	HL-60	blood:	n/a
26	chr5:98368443-98368493	HMEC	breast:	n/a
27	chr5:98541874-98541924	NB4	blood:	n/a
28	chr5:98746281-98746331	NHDF-neo	bronchial:	n/a
29	chr5:98541824-98541874	NT2-D1	testis:	n/a
30	chr5:98368443-98368493	PrEC	prostate:	n/a
31	chr5:98746281-98746331	GM06990	blood:	n/a
32	chr5:98541874-98541924	NHBE	bronchial:	n/a
33	chr5:98746281-98746331	HPAEpiC	pulmonary alveolar:	n/a
34	chr5:98860157-98860207	BJ	skin:	n/a
35	chr5:98541824-98541874	AG10803	skin:	n/a
36	chr5:98860157-98860207	Jurkat	blood:	n/a
37	chr5:98541824-98541874	HEEpiC	esophagus:	n/a
38	chr5:98541783-98541833	HCF	heart:	n/a
39	chr5:98541874-98541924	BJ	skin:	n/a
40	chr5:98541874-98541924	Caco-2	colon:	n/a
41	chr5:98396620-98396670	AG09319	gingival:	n/a
42	chr5:98541783-98541833	GM12891	blood:	n/a
43	chr5:98746281-98746331	AG04450	lung:	fetal
44	chr5:98368443-98368493	SK-N-SH	brain:	n/a
45	chr5:98368443-98368493	GM12878	blood:	n/a
46	chr5:98714340-98714390	T-47D	breast:	n/a
47	chr5:98746212-98746262	ECC-1	luminal epithelium:	n/a
48	chr5:98860157-98860207	AG04450	lung:	fetal
49	chr5:98860157-98860207	NHBE	bronchial:	n/a
50	chr5:98541824-98541874	IMR90	lung:	fetal

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:98439759..98440660-chr5:101559209..101559794,3	K562	blood:
2	chr5:98263067..98265701-chr5:98365532..98368540,4	MCF-7	breast:
3	chr5:98250951..98253126-chr5:98356611..98358893,2	K562	blood:
4	chr5:98429467..98432649-chr5:98432895..98434455,3	K562	blood:
5	chr5:98423960..98426113-chr5:98429583..98431463,3	K562	blood:
6	chr5:98936687..98938908-chr5:98939757..98941511,2	MCF-7	breast:
7	chr5:98254296..98256757-chr5:98393861..98395478,2	K562	blood:
8	chr5:98398453..98401255-chr5:98402077..98404728,2	K562	blood:
9	chr5:98461688..98463310-chr5:98465572..98467259,2	K562	blood:
10	chr5:98386273..98389246-chr5:98395943..98397711,2	K562	blood:
11	chr5:98243191..98245221-chr5:98386260..98388013,2	K562	blood:
12	chr5:98386273..98389246-chr5:98395943..98397711,2	K562	blood:
13	chr5:98439732..98443167-chr5:98443628..98446985,4	K562	blood:
14	chr5:98263522..98265138-chr5:98387990..98390059,2	K562	blood:
15	chr5:98641996..98644469-chr5:98647051..98649595,2	K562	blood:
16	chr5:98439732..98443167-chr5:98443628..98446985,4	K562	blood:
17	chr5:98264285..98266376-chr5:98383857..98386212,2	K562	blood:
18	chr5:98683331..98686253-chr5:98686370..98688077,2	K562	blood:
19	chr5:98263463..98264993-chr5:98394604..98397406,2	K562	blood:
20	chr5:98372764..98374577-chr5:98390711..98393548,2	MCF-7	breast:
21	chr5:97966444..97968012-chr5:98368423..98370387,2	K562	blood:
22	chr5:98367873..98368452-chr5:98395154..98396281,3	MCF-7	breast:
23	chr5:98367873..98368452-chr5:98395154..98396281,3	MCF-7	breast:
24	chr5:99005599..99009743-chr5:99010276..99013460,3	MCF-7	breast:
25	chr5:98263646..98265342-chr5:98360622..98362324,2	MCF-7	breast:
26	chr5:98423960..98426113-chr5:98429583..98431463,3	K562	blood:
27	chr5:98973640..98976479-chr5:98981401..98983390,2	MCF-7	breast:
28	chr5:98264688..98266479-chr5:98468438..98470812,2	K562	blood:
29	chr5:98264902..98266916-chr5:98381565..98384690,3	K562	blood:
30	chr5:98247883..98250755-chr5:98381007..98383241,2	K562	blood:
31	chr5:98240910..98242219-chr5:98367905..98368817,11	MCF-7	breast:
32	chr5:98356545..98359049-chr5:98366364..98368367,2	K562	blood:
33	chr5:98362205..98363958-chr5:98366950..98369649,2	MCF-7	breast:
34	chr5:98241174..98243544-chr5:98361759..98364961,3	K562	blood:
35	chr5:98382879..98385337-chr5:98386615..98388496,2	K562	blood:
36	chr5:98440206..98440855-chr5:98503610..98504175,2	MCF-7	breast:
37	chr5:98263162..98264704-chr5:98365544..98368385,2	K562	blood:
38	chr5:98380774..98382575-chr5:98387659..98389837,2	K562	blood:
39	chr5:98469162..98471809-chr5:98495145..98496723,2	K562	blood:
40	chr5:98411117..98412931-chr5:98414405..98417154,2	K562	blood:
41	chr5:98687563..98689159-chr5:98702688..98704857,2	MCF-7	breast:
42	chr5:98355578..98358107-chr5:98362158..98365732,4	K562	blood:
43	chr5:98252569..98255536-chr5:98389385..98390974,2	K562	blood:
44	chr5:98262538..98264376-chr5:98385068..98386574,2	K562	blood:
45	chr5:98369332..98370875-chr5:98373257..98375496,2	K562	blood:
46	chr5:98262156..98264317-chr5:98355438..98358771,4	K562	blood:
47	chr5:98304985..98305640-chr5:98368116..98368862,2	MCF-7	breast:
48	chr5:98266316..98268754-chr5:98386981..98389928,2	MCF-7	breast:
49	chr5:98380774..98382575-chr5:98387659..98389837,2	K562	blood:
50	chr5:98382879..98385337-chr5:98386615..98388496,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGMB-8	chr5:98825263-98825644	NONHSAT102979
2	lnc-RGMB-2	chr5:98885136-98885236	ENSG00000249515
3	lnc-RGMB-8	chr5:98834774-98835071	NONHSAT102979
4	lnc-RGMB-9	chr5:98930584-98931001	NONHSAT102983
5	lnc-CHD1-8	chr5:98930033-98930444	NONHSAT102982
6	lnc-RGMB-2	chr5:98913427-98913661	ENSG00000249515

No data

Variant related genes	Relation type
ENSG00000249444	TF binding region
ENSG00000206356	TF binding region
ENSG00000248236	TF binding region
ENSG00000248928	TF binding region
GUSBP8	TF binding region
ENSG00000249515	TF binding region
ENSG00000249444	CpG island
ENSG00000206356	CpG island
ENSG00000248236	CpG island
ENSG00000248928	CpG island
GUSBP8	CpG island
ENSG00000249515	CpG island
ENSG00000248489	chromatin interactions
ENSG00000048471	chromatin interactions
ENSG00000153922	chromatin interactions
ENSG00000166743	chromatin interactions
ENSG00000200351	chromatin interactions
ENSG00000234719	chromatin interactions

Extended variants
information (count: 7759 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:7759 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6878136	chr5:98358191-98358192	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371876153	chr5:98358212-98358213	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs192916090	chr5:98358240-98358241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs554955339	chr5:98358274-98358275	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535976415	chr5:98358278-98358279	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs183981802	chr5:98358303-98358304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575804637	chr5:98358384-98358385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542709879	chr5:98358389-98358390	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs6883467	chr5:98358396-98358397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs568616267	chr5:98358414-98358415	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145977418	chr5:98358431-98358432	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139849724	chr5:98358442-98358443	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559666159	chr5:98358497-98358498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10041263	chr5:98358562-98358563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs372667262	chr5:98358592-98358593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541428692	chr5:98358596-98358597	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557815857	chr5:98358616-98358617	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs10039507	chr5:98358698-98358699	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs543314934	chr5:98358721-98358722	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs189099363	chr5:98358727-98358728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149828770	chr5:98358744-98358745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567368980	chr5:98358780-98358781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534301752	chr5:98358787-98358788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563516615	chr5:98358807-98358808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546216693	chr5:98358813-98358814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200719200	chr5:98358819-98358820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs397781632	chr5:98358820-98358821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201803647	chr5:98358823-98358824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs72541057	chr5:98358830-98358831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397998825	chr5:98358831-98358832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201387228	chr5:98358833-98358834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10041335	chr5:98358852-98358853	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538906544	chr5:98358940-98358941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557637911	chr5:98359009-98359010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181486490	chr5:98359048-98359049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186394588	chr5:98359062-98359063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145843185	chr5:98359084-98359085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7723242	chr5:98359112-98359113	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs10041261	chr5:98359139-98359140	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs56086412	chr5:98359148-98359149	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs113267510	chr5:98359154-98359155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545273946	chr5:98359180-98359181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs563620997	chr5:98359239-98359240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530584004	chr5:98359252-98359253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542840475	chr5:98359285-98359286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs534277481	chr5:98359290-98359291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148585944	chr5:98359291-98359292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs570863709	chr5:98359301-98359302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532003026	chr5:98359332-98359333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs56115002	chr5:98359361-98359362	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	21248843	CNVD

Chromatin state (count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:98353600-98361600	Weak transcription	Small Intestine	intestine
2	chr5:98355000-98358200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr5:98355000-98358400	Enhancers	Fetal Intestine Small	intestine
4	chr5:98355000-98358600	Enhancers	Fetal Intestine Large	intestine
5	chr5:98355600-98358400	Enhancers	HepG2	liver
6	chr5:98356000-98360600	Weak transcription	Colonic Mucosa	Colon
7	chr5:98356400-98360400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr5:98356400-98360400	Weak transcription	GM12878-XiMat	blood
9	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells	blood
10	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr5:98356400-98361000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:98356400-98361200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr5:98356400-98361200	Weak transcription	Fetal Stomach	stomach
14	chr5:98356400-98361600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr5:98356400-98361800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr5:98356400-98362400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr5:98356800-98358200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr5:98356800-98361000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr5:98356800-98361000	Weak transcription	A549	lung
20	chr5:98356800-98361000	Weak transcription	HUVEC	blood vessel
21	chr5:98356800-98361200	Weak transcription	Adipose Nuclei	Adipose
22	chr5:98357000-98360200	Weak transcription	Liver	Liver
23	chr5:98357000-98360400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr5:98357000-98361200	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr5:98357000-98362000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr5:98357200-98358200	Enhancers	K562	blood
27	chr5:98357200-98360200	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr5:98357400-98360200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr5:98357400-98368400	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr5:98357600-98358800	Enhancers	Stomach Mucosa	stomach
31	chr5:98358000-98358400	Enhancers	Sigmoid Colon	Sigmoid Colon
32	chr5:98358200-98360000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr5:98358200-98366800	Weak transcription	K562	blood
34	chr5:98358400-98360000	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr5:98358400-98360000	Weak transcription	HepG2	liver
36	chr5:98358400-98360200	Weak transcription	Fetal Intestine Small	intestine
37	chr5:98358600-98360000	Weak transcription	Fetal Intestine Large	intestine
38	chr5:98358800-98360000	Weak transcription	Stomach Mucosa	stomach
39	chr5:98360000-98361400	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr5:98360000-98361800	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr5:98360000-98363200	Enhancers	Fetal Intestine Large	intestine
42	chr5:98360000-98363200	Enhancers	HepG2	liver
43	chr5:98360000-98363400	Enhancers	Stomach Mucosa	stomach
44	chr5:98360200-98361200	Enhancers	Liver	Liver
45	chr5:98360200-98361200	Enhancers	Rectal Mucosa Donor 29	rectum
46	chr5:98360200-98362800	Enhancers	Duodenum Mucosa	Duodenum
47	chr5:98360200-98362800	Enhancers	Pancreas	Pancrea
48	chr5:98360200-98363400	Enhancers	Fetal Intestine Small	intestine
49	chr5:98360200-98369000	Enhancers	Primary B cells from peripheral blood	blood
50	chr5:98360400-98362200	Enhancers	GM12878-XiMat	blood

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