Variant report

Variant	nsv1030036
Chromosome Location	chr5:179543546-179610871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:854)
CpG islands
(count:2320)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:179601223-179601365	K562	blood:	n/a	n/a
2	ATF3	chr5:179563820-179563990	K562	blood:	n/a	n/a
3	BACH1	chr5:179561454-179561491	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:179553967-179554302	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr5:179601267-179601897	GM12878	blood:	n/a	chr5:179601663-179601676
6	BCL3	chr5:179601323-179601671	GM12878	blood:	n/a	n/a
7	BHLHE40	chr5:179554169-179554355	K562	blood:	n/a	n/a
8	BHLHE40	chr5:179569016-179569216	K562	blood:	n/a	chr5:179569061-179569082 chr5:179569068-179569077
9	BHLHE40	chr5:179604518-179604553	K562	blood:	n/a	n/a
10	BHLHE40	chr5:179563858-179564016	K562	blood:	n/a	n/a
11	BHLHE40	chr5:179600029-179600349	HepG2	liver:	n/a	n/a
12	BHLHE40	chr5:179601408-179601608	K562	blood:	n/a	n/a
13	BRCA1	chr5:179544320-179544323	HepG2	liver:	n/a	n/a
14	BRCA1	chr5:179544235-179544409	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr5:179563853-179564104	K562	blood:	n/a	n/a
16	CCNT2	chr5:179545577-179545642	K562	blood:	n/a	n/a
17	CCNT2	chr5:179554101-179554301	K562	blood:	n/a	n/a
18	CEBPB	chr5:179549950-179550243	HepG2	liver:	n/a	chr5:179550134-179550145
19	CEBPB	chr5:179599972-179600343	HepG2	liver:	n/a	chr5:179600119-179600130
20	CEBPB	chr5:179591922-179592067	A549	lung:	n/a	n/a
21	CEBPB	chr5:179600034-179600223	A549	lung:	n/a	chr5:179600119-179600130
22	CEBPB	chr5:179549952-179550212	Hela-S3	cervix:	n/a	chr5:179550134-179550145
23	CEBPB	chr5:179599930-179600309	HepG2	liver:	n/a	chr5:179600119-179600130
24	CEBPB	chr5:179549912-179550228	IMR90	lung:	n/a	chr5:179550134-179550145
25	CEBPB	chr5:179552907-179553172	A549	lung:	n/a	chr5:179553078-179553091 chr5:179553057-179553068
26	CEBPB	chr5:179599877-179600339	MCF-7	breast:	n/a	chr5:179600119-179600130
27	CEBPB	chr5:179599936-179600312	HepG2	liver:	n/a	chr5:179600119-179600130
28	CEBPB	chr5:179544297-179544368	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr5:179549905-179550246	A549	lung:	n/a	chr5:179550134-179550145
30	CEBPB	chr5:179604282-179604596	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:179554149-179554313	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr5:179549944-179550090	K562	blood:	n/a	n/a
33	CEBPB	chr5:179552950-179553146	HepG2	liver:	n/a	chr5:179553078-179553091 chr5:179553057-179553068
34	CEBPB	chr5:179604308-179604523	HepG2	liver:	n/a	n/a
35	CEBPB	chr5:179599982-179600245	HepG2	liver:	n/a	chr5:179600119-179600130
36	CEBPB	chr5:179553011-179553105	IMR90	lung:	n/a	chr5:179553078-179553091 chr5:179553057-179553068
37	CEBPB	chr5:179583154-179583357	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPD	chr5:179599968-179600197	HepG2	liver:	n/a	n/a
39	CHD1	chr5:179553815-179554505	IMR90	lung:	n/a	n/a
40	CHD2	chr5:179554037-179554206	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr5:179544368-179544453	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr5:179604506-179604549	HepG2	liver:	n/a	n/a
43	CREB1	chr5:179554039-179554393	A549	lung:	n/a	n/a
44	CTCF	chr5:179554100-179554250	WI-38	lung:	n/a	chr5:179554211-179554224 chr5:179554212-179554230
45	CTCF	chr5:179589014-179589263	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:179554140-179554290	WI-38	lung:	n/a	chr5:179554275-179554288 chr5:179554211-179554224 chr5:179554212-179554230
47	CTCF	chr5:179583231-179583340	Fibrobl	skin:	n/a	chr5:179583260-179583269
48	CTCF	chr5:179583220-179583370	K562	blood:	n/a	chr5:179583260-179583269
49	CTCF	chr5:179583148-179583395	H1-hESC	embryonic stem cell:	n/a	chr5:179583211-179583224 chr5:179583260-179583269
50	CTCF	chr5:179589054-179589230	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179563745-179563795	AG04450	lung:	fetal
2	chr5:179566792-179566842	H1-hESC	embryonic stem cell:	embryo
3	chr5:179563745-179563795	AG04450	lung:	fetal
4	chr5:179566792-179566842	H1-hESC	embryonic stem cell:	embryo
5	chr5:179563497-179563547	HNPCEpiC	eye:	n/a
6	chr5:179564602-179564652	IMR90	lung:	fetal
7	chr5:179554466-179554516	SK-N-SH	brain:	n/a
8	chr5:179597526-179597576	HRCEpiC	kidney:	n/a
9	chr5:179566792-179566842	T-47D	breast:	n/a
10	chr5:179565362-179565412	CMK	blood:	n/a
11	chr5:179598884-179598934	HCT-116	colon:	n/a
12	chr5:179565362-179565412	RPTEC	kidney:	n/a
13	chr5:179565362-179565412	ECC-1	luminal epithelium:	n/a
14	chr5:179554466-179554516	Caco-2	colon:	n/a
15	chr5:179585198-179585248	SK-N-MC	brain:	n/a
16	chr5:179563839-179563889	AG10803	skin:	n/a
17	chr5:179591070-179591120	Hela-S3	cervix:	n/a
18	chr5:179587950-179588000	IMR90	lung:	fetal
19	chr5:179563866-179563916	HEEpiC	esophagus:	n/a
20	chr5:179565349-179565399	LNCaP	prostate:	n/a
21	chr5:179557008-179557058	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:179602982-179603032	NB4	blood:	n/a
23	chr5:179588838-179588888	HEEpiC	esophagus:	n/a
24	chr5:179602982-179603032	HRCEpiC	kidney:	n/a
25	chr5:179559290-179559340	HUVEC	blood vessel:	n/a
26	chr5:179563497-179563547	HEEpiC	esophagus:	n/a
27	chr5:179588440-179588490	ECC-1	luminal epithelium:	n/a
28	chr5:179602982-179603032	BJ	skin:	n/a
29	chr5:179564602-179564652	Caco-2	colon:	n/a
30	chr5:179563896-179563946	AG04449	skin:	fetal
31	chr5:179554555-179554605	RPTEC	kidney:	n/a
32	chr5:179588673-179588723	HUVEC	blood vessel:	n/a
33	chr5:179563839-179563889	LNCaP	prostate:	n/a
34	chr5:179562118-179562168	GM12878	blood:	n/a
35	chr5:179562118-179562168	AG10803	skin:	n/a
36	chr5:179563866-179563916	HCPEpiC	choroid plexus:	n/a
37	chr5:179588838-179588888	SK-N-SH_RA	brain:	n/a
38	chr5:179553589-179553639	NB4	blood:	n/a
39	chr5:179588551-179588601	AoSMC	blood vessel:	n/a
40	chr5:179565349-179565399	GM12892	blood:	n/a
41	chr5:179565544-179565594	K562	blood:	n/a
42	chr5:179588673-179588723	HCF	heart:	n/a
43	chr5:179591070-179591120	HRCEpiC	kidney:	n/a
44	chr5:179597526-179597576	HCPEpiC	choroid plexus:	n/a
45	chr5:179565349-179565399	PANC-1	pancreas:	n/a
46	chr5:179563745-179563795	HUVEC	blood vessel:	n/a
47	chr5:179564602-179564652	HEK293	kidney:	embryo
48	chr5:179563200-179563250	MCF-7	breast:	n/a
49	chr5:179602982-179603032	HCT-116	colon:	n/a
50	chr5:179563745-179563795	HIPEpiC	eye:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:179544196..179547081-chr5:179550763..179552798,2	MCF-7	breast:
2	chr5:179551929..179554732-chr5:179557989..179560690,2	K562	blood:
3	chr5:179551435..179553864-chr5:179559199..179562159,2	K562	blood:
4	chr5:179556597..179557163-chr5:179565658..179566414,2	MCF-7	breast:
5	chr5:179594862..179596612-chr5:179598475..179600165,2	MCF-7	breast:
6	chr5:179555641..179558112-chr5:179558686..179561172,2	K562	blood:
7	chr5:179603344..179605727-chr5:179894143..179896109,2	K562	blood:
8	chr5:179544196..179547081-chr5:179550763..179552798,2	MCF-7	breast:
9	chr5:179588724..179589352-chr5:179627753..179628617,2	MCF-7	breast:
10	chr5:179539744..179541292-chr5:179548129..179549893,2	K562	blood:
11	chr5:179560653..179562263-chr5:179716326..179719288,2	MCF-7	breast:
12	chr5:179598097..179600752-chr5:179603179..179605823,2	K562	blood:
13	chr5:179497086..179499283-chr5:179543542..179545830,3	MCF-7	breast:
14	chr5:179598097..179600752-chr5:179603179..179605823,2	K562	blood:
15	chr5:179523738..179525811-chr5:179544274..179545923,2	MCF-7	breast:
16	chr5:179539744..179542494-chr5:179548129..179549893,3	K562	blood:
17	chr5:179565014..179567523-chr5:179570668..179572800,2	K562	blood:
18	chr5:179553754..179554423-chr5:179720168..179720917,3	MCF-7	breast:
19	chr5:179561122..179566111-chr5:179566279..179570642,6	MCF-7	breast:
20	chr5:179543851..179544407-chr5:179635297..179636277,2	MCF-7	breast:
21	chr5:179558293..179560674-chr5:179562402..179565370,2	MCF-7	breast:
22	chr5:179555641..179558112-chr5:179558686..179561172,2	K562	blood:
23	chr5:179546334..179548220-chr5:179553814..179555869,2	MCF-7	breast:
24	chr5:179598082..179600622-chr5:179601152..179603406,2	K562	blood:
25	chr5:179554088..179554742-chr5:179742467..179743013,2	MCF-7	breast:
26	chr5:179551435..179553864-chr5:179559199..179562159,2	K562	blood:
27	chr5:179553629..179554257-chr5:179627968..179628886,2	MCF-7	breast:
28	chr5:179553532..179554679-chr5:179635533..179636665,15	MCF-7	breast:
29	chr5:179594862..179596612-chr5:179598475..179600165,2	MCF-7	breast:
30	chr5:179544274..179545099-chr5:179553728..179554648,2	MCF-7	breast:
31	chr5:179546163..179549028-chr5:179553453..179555820,2	K562	blood:
32	chr5:179553744..179554692-chr5:180097393..180098230,2	MCF-7	breast:
33	chr5:179601654..179603372-chr5:179739320..179741770,2	MCF-7	breast:
34	chr5:179553781..179554858-chr5:179635686..179636541,5	MCF-7	breast:
35	chr5:179554536..179556521-chr5:179716236..179718994,2	MCF-7	breast:
36	chr5:179542665..179545616-chr5:179718276..179721972,3	MCF-7	breast:
37	chr5:179556597..179557163-chr5:179565658..179566414,2	MCF-7	breast:
38	chr5:179551929..179554732-chr5:179557989..179560690,2	K562	blood:
39	chr5:179546163..179549028-chr5:179553453..179555820,2	K562	blood:
40	chr5:179546334..179548220-chr5:179553814..179555869,2	MCF-7	breast:
41	chr5:179568439..179571185-chr5:179571573..179574464,2	K562	blood:
42	chr5:179562265..179564254-chr5:179568163..179570454,2	K562	blood:
43	chr5:179568439..179571185-chr5:179571573..179574464,2	K562	blood:
44	chr5:179598082..179600622-chr5:179601152..179603406,2	K562	blood:
45	chr5:179544274..179545099-chr5:179553728..179554648,2	MCF-7	breast:
46	chr5:179553164..179556296-chr5:179740039..179742529,3	MCF-7	breast:

No data

Variant related genes	Relation type
RASGEF1C	TF binding region
RASGEF1C	CpG island
ENSG00000050748	chromatin interactions
ENSG00000113269	chromatin interactions
ENSG00000146090	chromatin interactions
ENSG00000248367	chromatin interactions

Extended variants
information (count: 2800 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2800 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11741189	chr5:179543546-179543547	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs543876233	chr5:179543547-179543548	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs562148216	chr5:179543575-179543576	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs574055488	chr5:179543579-179543580	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs563873466	chr5:179543580-179543581	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs190401667	chr5:179543584-179543585	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs181373413	chr5:179543696-179543697	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs10041337	chr5:179543703-179543704	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs565441559	chr5:179543708-179543709	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs532672654	chr5:179543709-179543710	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs551046069	chr5:179543714-179543715	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs569282524	chr5:179543731-179543732	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs148797554	chr5:179543739-179543740	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs529474634	chr5:179543769-179543770	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs12656413	chr5:179543811-179543812	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs566632825	chr5:179543909-179543910	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs534060703	chr5:179543948-179543949	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs558494779	chr5:179544069-179544070	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs570663625	chr5:179544100-179544101	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs114198336	chr5:179544101-179544102	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs539692360	chr5:179544122-179544123	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs184020390	chr5:179544250-179544251	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs549060968	chr5:179544260-179544261	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs541442183	chr5:179544304-179544305	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs561663552	chr5:179544320-179544321	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs74397919	chr5:179544336-179544337	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs573471666	chr5:179544341-179544342	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs142435075	chr5:179544366-179544367	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs60425482	chr5:179544385-179544386	Weak transcription Enhancers Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs188407889	chr5:179544432-179544433	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs150881380	chr5:179544480-179544481	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs550595740	chr5:179544481-179544482	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs551136177	chr5:179544502-179544503	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs78011085	chr5:179544546-179544547	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs560246933	chr5:179544572-179544573	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs530136366	chr5:179544644-179544645	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs559459650	chr5:179544660-179544661	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs114343131	chr5:179544661-179544662	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs376589071	chr5:179544669-179544670	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs555769093	chr5:179544670-179544671	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs60610690	chr5:179544673-179544674	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs4451016	chr5:179544678-179544679	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs572486149	chr5:179544685-179544686	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs139342697	chr5:179544696-179544697	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs148504909	chr5:179544711-179544712	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs180922106	chr5:179544719-179544720	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs186189719	chr5:179544722-179544723	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs535502805	chr5:179544723-179544724	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs553512548	chr5:179544731-179544732	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs112888445	chr5:179544732-179544733	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
small cell lung cancer	20016488	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:697 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179536000-179543600	Weak transcription	Fetal Brain Female	brain
2	chr5:179536200-179554200	Weak transcription	Brain Germinal Matrix	brain
3	chr5:179537800-179546000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:179539000-179545000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr5:179542600-179544000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr5:179542800-179543800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:179542800-179543800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr5:179543000-179543800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:179543000-179543800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:179543000-179544000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr5:179543000-179544000	Enhancers	Brain Hippocampus Middle	brain
12	chr5:179543000-179544000	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr5:179543000-179544400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:179543200-179543800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chr5:179543200-179543800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:179543200-179543800	Enhancers	Brain Anterior Caudate	brain
17	chr5:179543200-179544000	Enhancers	Brain Angular Gyrus	brain
18	chr5:179543200-179544400	Enhancers	Brain Substantia Nigra	brain
19	chr5:179543200-179545200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:179543400-179543800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr5:179543400-179544000	Enhancers	Brain Cingulate Gyrus	brain
22	chr5:179543400-179553800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr5:179543600-179548000	Strong transcription	Fetal Brain Female	brain
24	chr5:179543800-179544600	Enhancers	Esophagus	oesophagus
25	chr5:179543800-179545400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr5:179543800-179548800	Weak transcription	Brain Anterior Caudate	brain
27	chr5:179544000-179544600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr5:179544000-179548600	Weak transcription	Brain Hippocampus Middle	brain
29	chr5:179544000-179548800	Weak transcription	Brain Angular Gyrus	brain
30	chr5:179544000-179553800	Weak transcription	Brain Cingulate Gyrus	brain
31	chr5:179544000-179554000	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr5:179544200-179544400	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:179544400-179545400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:179544400-179548800	Weak transcription	Brain Substantia Nigra	brain
35	chr5:179545200-179545400	Enhancers	K562	blood
36	chr5:179545200-179545600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:179545400-179545600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr5:179545400-179546400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:179545600-179553600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr5:179546400-179547400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:179547200-179548200	Enhancers	Pancreas	Pancrea
42	chr5:179547400-179548000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:179547600-179548000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr5:179548000-179553800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr5:179548000-179558800	Weak transcription	Fetal Brain Female	brain
46	chr5:179548600-179549000	Enhancers	Brain Hippocampus Middle	brain
47	chr5:179548800-179549200	Enhancers	Brain Anterior Caudate	brain
48	chr5:179548800-179549400	Enhancers	Brain Angular Gyrus	brain
49	chr5:179548800-179549400	Enhancers	Brain Substantia Nigra	brain
50	chr5:179549400-179549600	Enhancers	Placenta	Placenta

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