Variant report

Variant	nsv883213
Chromosome Location	chr5:177811754-177947771
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1195)
CpG islands
(count:3052)
Chromatin interactive
region (count:85)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1195 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:177877562-177878156	K562	blood:	n/a	n/a
2	ARID3A	chr5:177844349-177844766	K562	blood:	n/a	n/a
3	ARID3A	chr5:177888233-177888383	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:177875635-177876882	K562	blood:	n/a	n/a
5	ARID3A	chr5:177880009-177880448	K562	blood:	n/a	n/a
6	ATF1	chr5:177914943-177915183	K562	blood:	n/a	n/a
7	ATF1	chr5:177844242-177844772	K562	blood:	n/a	n/a
8	ATF1	chr5:177876057-177876633	K562	blood:	n/a	n/a
9	BACH1	chr5:177920408-177920532	K562	blood:	n/a	n/a
10	BACH1	chr5:177934563-177934814	K562	blood:	n/a	n/a
11	BACH1	chr5:177876133-177876859	K562	blood:	n/a	n/a
12	BACH1	chr5:177844549-177844755	K562	blood:	n/a	n/a
13	BACH1	chr5:177869383-177869508	K562	blood:	n/a	n/a
14	BACH1	chr5:177886021-177886090	K562	blood:	n/a	n/a
15	BACH1	chr5:177872621-177872910	K562	blood:	n/a	n/a
16	BACH1	chr5:177888080-177888450	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCLAF1	chr5:177876134-177876491	K562	blood:	n/a	n/a
18	BHLHE40	chr5:177888120-177888558	K562	blood:	n/a	n/a
19	BHLHE40	chr5:177921213-177921579	K562	blood:	n/a	n/a
20	BHLHE40	chr5:177895932-177896151	K562	blood:	n/a	n/a
21	BHLHE40	chr5:177847184-177847250	K562	blood:	n/a	n/a
22	BHLHE40	chr5:177930090-177930416	K562	blood:	n/a	n/a
23	BHLHE40	chr5:177826063-177826418	K562	blood:	n/a	chr5:177826237-177826250
24	BHLHE40	chr5:177844227-177844729	K562	blood:	n/a	n/a
25	BHLHE40	chr5:177918301-177918460	K562	blood:	n/a	chr5:177918370-177918383
26	BHLHE40	chr5:177910649-177910918	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:177929771-177930071	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:177880099-177880651	K562	blood:	n/a	n/a
29	BHLHE40	chr5:177910645-177910908	K562	blood:	n/a	n/a
30	BHLHE40	chr5:177934517-177934717	K562	blood:	n/a	n/a
31	BHLHE40	chr5:177876113-177877870	K562	blood:	n/a	n/a
32	BRCA1	chr5:177888202-177888501	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr5:177888215-177888415	HepG2	liver:	n/a	n/a
34	CBX3	chr5:177876066-177876600	K562	blood:	n/a	n/a
35	CBX3	chr5:177876014-177876642	K562	blood:	n/a	n/a
36	CBX3	chr5:177934495-177934851	K562	blood:	n/a	n/a
37	CBX3	chr5:177934424-177934912	K562	blood:	n/a	n/a
38	CCNT2	chr5:177869079-177869128	K562	blood:	n/a	n/a
39	CCNT2	chr5:177844365-177844831	K562	blood:	n/a	n/a
40	CCNT2	chr5:177882316-177882695	K562	blood:	n/a	n/a
41	CCNT2	chr5:177876058-177876813	K562	blood:	n/a	chr5:177876543-177876552 chr5:177876671-177876680 chr5:177876666-177876675
42	CCNT2	chr5:177877417-177877873	K562	blood:	n/a	n/a
43	CCNT2	chr5:177840401-177840601	K562	blood:	n/a	n/a
44	CEBPB	chr5:177914903-177915241	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr5:177938843-177939377	HepG2	liver:	n/a	chr5:177939287-177939298
46	CEBPB	chr5:177902447-177902754	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:177857365-177857496	K562	blood:	n/a	chr5:177857389-177857398 chr5:177857387-177857398 chr5:177857389-177857400
48	CEBPB	chr5:177876177-177876424	K562	blood:	n/a	n/a
49	CEBPB	chr5:177914818-177915372	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr5:177857305-177857528	Hela-S3	cervix:	n/a	chr5:177857389-177857398 chr5:177857387-177857398 chr5:177857389-177857400

(count:3052 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:177819485-177819535	A549	lung:	n/a
2	chr5:177821870-177821920	MCF10A-Er-Src	breast:	n/a
3	chr5:177819485-177819535	A549	lung:	n/a
4	chr5:177821870-177821920	MCF10A-Er-Src	breast:	n/a
5	chr5:177890863-177890913	NH-A	brain:	n/a
6	chr5:177913485-177913535	HAEpiC	amniotic membrane:	n/a
7	chr5:177823864-177823914	AG04449	skin:	fetal
8	chr5:177892758-177892808	NB4	blood:	n/a
9	chr5:177941879-177941929	NB4	blood:	n/a
10	chr5:177823864-177823914	ProgFib	skin:	n/a
11	chr5:177814702-177814752	HCPEpiC	choroid plexus:	n/a
12	chr5:177913434-177913484	NH-A	brain:	n/a
13	chr5:177821870-177821920	AG09319	gingival:	n/a
14	chr5:177825282-177825332	T-47D	breast:	n/a
15	chr5:177929948-177929998	PANC-1	pancreas:	n/a
16	chr5:177913468-177913518	SKMC	muscle:	n/a
17	chr5:177941879-177941929	SAEC	small airway:	n/a
18	chr5:177941617-177941667	AG10803	skin:	n/a
19	chr5:177892758-177892808	HAEpiC	amniotic membrane:	n/a
20	chr5:177824403-177824453	HIPEpiC	eye:	n/a
21	chr5:177892911-177892961	U87	brain:	n/a
22	chr5:177889945-177889995	AG09309	skin:	n/a
23	chr5:177823856-177823906	AG09309	skin:	n/a
24	chr5:177947425-177947475	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:177892758-177892808	SAEC	small airway:	n/a
26	chr5:177890816-177890866	NT2-D1	testis:	n/a
27	chr5:177875140-177875190	T-47D	breast:	n/a
28	chr5:177929948-177929998	AG10803	skin:	n/a
29	chr5:177891151-177891201	HIPEpiC	eye:	n/a
30	chr5:177947425-177947475	HUVEC	blood vessel:	n/a
31	chr5:177895047-177895097	AG09309	skin:	n/a
32	chr5:177819485-177819535	BJ	skin:	n/a
33	chr5:177891221-177891271	MCF10A-Er-Src	breast:	n/a
34	chr5:177916395-177916445	Caco-2	colon:	n/a
35	chr5:177941879-177941929	GM12891	blood:	n/a
36	chr5:177891151-177891201	Hela-S3	cervix:	n/a
37	chr5:177913434-177913484	HAEpiC	amniotic membrane:	n/a
38	chr5:177942470-177942520	HepG2	liver:	n/a
39	chr5:177876930-177876980	GM12878	blood:	n/a
40	chr5:177827484-177827534	ECC-1	luminal epithelium:	n/a
41	chr5:177890603-177890653	NT2-D1	testis:	n/a
42	chr5:177814702-177814752	PrEC	prostate:	n/a
43	chr5:177890603-177890653	HIPEpiC	eye:	n/a
44	chr5:177824353-177824403	HCPEpiC	choroid plexus:	n/a
45	chr5:177882205-177882255	T-47D	breast:	n/a
46	chr5:177821870-177821920	GM12878	blood:	n/a
47	chr5:177929948-177929998	HCF	heart:	n/a
48	chr5:177913485-177913535	AG09309	skin:	n/a
49	chr5:177821870-177821920	PFSK-1	brain:	n/a
50	chr5:177941617-177941667	BE2_C	brain:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:177768665..177770480-chr5:177878843..177880879,2	K562	blood:
2	chr5:177882178..177883994-chr5:177886180..177888676,2	K562	blood:
3	chr5:177843982..177846399-chr5:177848195..177849989,2	MCF-7	breast:
4	chr5:177838677..177840723-chr5:177850329..177853314,2	K562	blood:
5	chr5:177841800..177844284-chr5:177969427..177971380,2	K562	blood:
6	chr5:177882178..177883994-chr5:177886180..177888676,2	K562	blood:
7	chr5:177876265..177878231-chr5:177880241..177881910,2	K562	blood:
8	chr5:177879706..177881386-chr5:177883345..177884930,2	K562	blood:
9	chr5:177933177..177935280-chr5:177937428..177940309,2	MCF-7	breast:
10	chr5:177893036..177895122-chr5:177964444..177967291,2	K562	blood:
11	chr5:177864722..177866446-chr5:177868114..177869710,2	K562	blood:
12	chr5:177940111..177942825-chr5:177947320..177948869,2	MCF-7	breast:
13	chr5:177879886..177881970-chr5:177890471..177892015,2	K562	blood:
14	chr5:177863976..177865906-chr5:177865925..177867596,2	MCF-7	breast:
15	chr5:177894292..177896063-chr5:177897258..177899224,2	K562	blood:
16	chr15:91426417..91426918-chr5:177903850..177904350,2	NB4	blood:
17	chr5:177861712..177865085-chr5:177866946..177869684,3	K562	blood:
18	chr5:177887805..177889193-chr5:178016576..178017370,3	MCF-7	breast:
19	chr5:177811102..177812638-chr5:177817501..177819406,2	K562	blood:
20	chr5:177846034..177846976-chr5:177861076..177861723,3	MCF-7	breast:
21	chr5:177873433..177876156-chr5:177880110..177882555,2	K562	blood:
22	chr5:177881991..177885625-chr5:177886030..177888202,3	MCF-7	breast:
23	chr5:177876012..177877743-chr5:177880216..177882479,2	MCF-7	breast:
24	chr5:177915163..177917911-chr5:177920254..177922621,2	K562	blood:
25	chr5:177764211..177766744-chr5:177842337..177844246,2	MCF-7	breast:
26	chr5:177844389..177846173-chr5:177851202..177854065,2	MCF-7	breast:
27	chr5:177940111..177942825-chr5:177947320..177948869,2	MCF-7	breast:
28	chr5:177816543..177819082-chr5:177820341..177823036,2	K562	blood:
29	chr5:177915163..177917911-chr5:177920254..177922621,2	K562	blood:
30	chr5:177871515..177874034-chr5:177875821..177877688,2	MCF-7	breast:
31	chr5:177892314..177894580-chr5:177899757..177901738,2	K562	blood:
32	chr5:177912045..177914389-chr5:177919098..177921696,2	MCF-7	breast:
33	chr5:177888015..177888839-chr5:177977833..177978735,3	MCF-7	breast:
34	chr5:177855622..177857824-chr5:177858602..177861991,3	K562	blood:
35	chr5:177887745..177890184-chr5:177903224..177905118,2	K562	blood:
36	chr5:177888252..177888759-chr5:177978244..177978784,2	K562	blood:
37	chr5:177876786..177879529-chr5:177883377..177886367,2	K562	blood:
38	chr5:177871515..177874034-chr5:177875821..177877688,2	MCF-7	breast:
39	chr5:177879886..177881970-chr5:177890471..177892015,2	K562	blood:
40	chr5:177892314..177894580-chr5:177899757..177901738,2	K562	blood:
41	chr5:177844557..177846538-chr5:177860811..177863618,2	K562	blood:
42	chr5:177861712..177864496-chr5:177868184..177871226,3	K562	blood:
43	chr5:177861063..177863215-chr5:177895852..177898464,2	K562	blood:
44	chr5:177851551..177854301-chr5:177861521..177864094,2	MCF-7	breast:
45	chr5:177811102..177814167-chr5:177815792..177819406,4	K562	blood:
46	chr5:177887719..177888721-chr5:177977307..177978270,3	MCF-7	breast:
47	chr5:177780201..177782328-chr5:177897256..177899348,2	MCF-7	breast:
48	chr5:177851066..177853109-chr5:177854719..177857640,2	MCF-7	breast:
49	chr5:177876012..177877743-chr5:177880216..177882479,2	MCF-7	breast:
50	chr5:177811102..177814167-chr5:177815792..177819406,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLK4-1	chr5:177869927-177870095	ENSG00000245688.1
2	lnc-CLK4-1	chr5:177865682-177866970	ENSG00000245688.1

No data

Variant related genes	Relation type
ENSG00000245688	TF binding region
ENSG00000245688	CpG island
ENSG00000245688	chromatin interactions

Extended variants
information (count: 5685 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5685 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13178731	chr5:177811754-177811755	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147838911	chr5:177811755-177811756	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537558845	chr5:177811756-177811757	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377586591	chr5:177811853-177811854	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78443836	chr5:177811874-177811875	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs113706596	chr5:177811892-177811893	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73803007	chr5:177811916-177811917	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572137788	chr5:177811917-177811918	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113207807	chr5:177811925-177811926	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557669908	chr5:177811926-177811927	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577224791	chr5:177811965-177811966	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544730717	chr5:177811984-177811985	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77030309	chr5:177811998-177811999	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115764288	chr5:177812004-177812005	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117548942	chr5:177812030-177812031	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181333260	chr5:177812037-177812038	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141480722	chr5:177812038-177812039	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552699530	chr5:177812048-177812049	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73803008	chr5:177812063-177812064	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531278122	chr5:177812105-177812106	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549493376	chr5:177812123-177812124	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545469994	chr5:177812125-177812126	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146982862	chr5:177812195-177812196	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547371725	chr5:177812196-177812197	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185579698	chr5:177812255-177812256	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs376944321	chr5:177812256-177812257	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539358083	chr5:177812262-177812263	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557899295	chr5:177812290-177812291	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562846547	chr5:177812291-177812292	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13160887	chr5:177812311-177812312	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs538328445	chr5:177812313-177812314	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577939914	chr5:177812314-177812315	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35627683	chr5:177812341-177812342	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556736686	chr5:177812359-177812360	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs80193995	chr5:177812360-177812361	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543863347	chr5:177812382-177812383	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560295247	chr5:177812424-177812425	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572664621	chr5:177812492-177812493	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371616131	chr5:177812499-177812500	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541655940	chr5:177812547-177812548	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11955873	chr5:177812552-177812553	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564681943	chr5:177812563-177812564	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs72822856	chr5:177812584-177812585	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs556239611	chr5:177812591-177812592	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549454711	chr5:177812596-177812597	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs62389383	chr5:177812611-177812612	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs113008864	chr5:177812621-177812622	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs541468276	chr5:177812627-177812628	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs2973733	chr5:177812641-177812642	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs527527676	chr5:177812686-177812687	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Thoracic aortic aneurysm	21092924	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
small cell lung cancer	20016488	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1495 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177798800-177816400	Weak transcription	Right Atrium	heart
2	chr5:177804800-177812800	Weak transcription	Spleen	Spleen
3	chr5:177805000-177814800	Weak transcription	Gastric	stomach
4	chr5:177808000-177815200	Bivalent Enhancer	Fetal Stomach	stomach
5	chr5:177808800-177812600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr5:177809200-177811800	Enhancers	Fetal Brain Male	brain
7	chr5:177809200-177812800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:177809400-177812200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:177809400-177813000	Enhancers	H1 Cell Line	embryonic stem cell
10	chr5:177809600-177812400	Enhancers	Fetal Heart	heart
11	chr5:177809600-177812800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr5:177809600-177815400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:177809600-177820400	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr5:177809800-177819400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr5:177810000-177812800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr5:177810200-177811800	Bivalent Enhancer	Fetal Intestine Large	intestine
17	chr5:177810200-177812000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:177810200-177812800	Bivalent Enhancer	Fetal Lung	lung
19	chr5:177810400-177812000	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr5:177810400-177812600	Bivalent Enhancer	Placenta	Placenta
21	chr5:177810400-177812600	Genic enhancers	Thymus	Thymus
22	chr5:177810800-177811800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
23	chr5:177810800-177815400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr5:177811000-177811800	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr5:177811000-177811800	Enhancers	Esophagus	oesophagus
26	chr5:177811000-177821400	Enhancers	Fetal Thymus	thymus
27	chr5:177811200-177811800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr5:177811200-177812000	Enhancers	Right Ventricle	heart
29	chr5:177811200-177814800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr5:177811600-177811800	Enhancers	Left Ventricle	heart
31	chr5:177811600-177812200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr5:177811600-177812200	Enhancers	Brain Germinal Matrix	brain
33	chr5:177811600-177812800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr5:177811600-177815200	Enhancers	Dnd41	blood
35	chr5:177811600-177821000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr5:177811800-177812000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
37	chr5:177811800-177817400	Weak transcription	Esophagus	oesophagus
38	chr5:177812000-177812200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
39	chr5:177812000-177813200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr5:177812000-177813800	Weak transcription	Right Ventricle	heart
41	chr5:177812200-177812400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr5:177812200-177812400	Enhancers	Primary B cells from cord blood	blood
43	chr5:177812200-177812400	Bivalent Enhancer	Fetal Intestine Small	intestine
44	chr5:177812200-177812600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr5:177812200-177812600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr5:177812200-177813600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:177812400-177812600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr5:177812400-177813000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:177812400-177813600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr5:177812600-177813000	Enhancers	Thymus	Thymus

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