Variant report

Variant	nsv882384
Chromosome Location	chr5:93136661-93380123
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1769)
CpG islands
(count:305)
Chromatin interactive
region (count:50)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:93136931-93137325	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:93245172-93245352	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:93240699-93241011	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:93361549-93361919	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:93234553-93235126	HepG2	liver:	n/a	chr5:93234774-93234790
6	ARID3A	chr5:93357018-93357302	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:93237936-93238452	HepG2	liver:	n/a	n/a
8	ATF1	chr5:93270400-93270423	K562	blood:	n/a	n/a
9	ATF1	chr5:93222200-93222335	K562	blood:	n/a	n/a
10	ATF1	chr5:93251048-93251117	K562	blood:	n/a	n/a
11	ATF1	chr5:93161939-93161960	K562	blood:	n/a	n/a
12	ATF2	chr5:93330929-93331346	GM12878	blood:	n/a	n/a
13	ATF3	chr5:93356892-93357426	A549	lung:	n/a	n/a
14	BATF	chr5:93160510-93160750	GM12878	blood:	n/a	n/a
15	BATF	chr5:93330960-93331283	GM12878	blood:	n/a	n/a
16	BATF	chr5:93209748-93210171	GM12878	blood:	n/a	chr5:93209951-93209962
17	BATF	chr5:93330901-93331363	GM12878	blood:	n/a	n/a
18	BATF	chr5:93209773-93210137	GM12878	blood:	n/a	chr5:93209951-93209962
19	BCL11A	chr5:93330990-93331206	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:93331008-93331267	GM12878	blood:	n/a	n/a
21	BCL3	chr5:93356878-93357473	A549	lung:	n/a	n/a
22	BCL3	chr5:93356837-93357419	A549	lung:	n/a	n/a
23	BHLHE40	chr5:93250882-93251070	GM12878	blood:	n/a	n/a
24	BHLHE40	chr5:93330740-93331199	GM12878	blood:	n/a	n/a
25	BHLHE40	chr5:93373375-93373400	GM12878	blood:	n/a	n/a
26	BRCA1	chr5:93136794-93137257	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr5:93250709-93251270	HCT-116	colon:	n/a	n/a
28	CBX3	chr5:93356779-93357558	HCT-116	colon:	n/a	n/a
29	CCNT2	chr5:93275858-93275919	K562	blood:	n/a	n/a
30	CEBPB	chr5:93326225-93326456	HepG2	liver:	n/a	chr5:93326350-93326361
31	CEBPB	chr5:93356906-93357497	A549	lung:	n/a	n/a
32	CEBPB	chr5:93261058-93261404	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr5:93222093-93222416	MCF-7	breast:	n/a	chr5:93222296-93222307
34	CEBPB	chr5:93222125-93222467	HepG2	liver:	n/a	chr5:93222422-93222435 chr5:93222296-93222307
35	CEBPB	chr5:93222230-93222381	H1-hESC	embryonic stem cell:	n/a	chr5:93222296-93222307
36	CEBPB	chr5:93199321-93199521	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr5:93287574-93287745	HepG2	liver:	n/a	n/a
38	CEBPB	chr5:93361555-93361928	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:93236425-93236601	IMR90	lung:	n/a	chr5:93236504-93236517 chr5:93236505-93236516 chr5:93236555-93236566 chr5:93236504-93236515
40	CEBPB	chr5:93217106-93217324	IMR90	lung:	n/a	n/a
41	CEBPB	chr5:93277744-93277944	HepG2	liver:	n/a	chr5:93277824-93277835
42	CEBPB	chr5:93240807-93240960	A549	lung:	n/a	chr5:93240925-93240934 chr5:93240818-93240831 chr5:93240923-93240934
43	CEBPB	chr5:93141495-93141875	IMR90	lung:	n/a	chr5:93141764-93141777 chr5:93141764-93141777 chr5:93141764-93141775 chr5:93141764-93141777
44	CEBPB	chr5:93348825-93349045	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr5:93222120-93222477	IMR90	lung:	n/a	chr5:93222422-93222435 chr5:93222296-93222307
46	CEBPB	chr5:93236438-93236655	HepG2	liver:	n/a	chr5:93236504-93236517 chr5:93236505-93236516 chr5:93236555-93236566 chr5:93236504-93236515
47	CEBPB	chr5:93228927-93229114	HepG2	liver:	n/a	chr5:93228986-93228997
48	CEBPB	chr5:93356722-93357528	HCT-116	colon:	n/a	n/a
49	CEBPB	chr5:93277674-93277855	H1-hESC	embryonic stem cell:	n/a	chr5:93277824-93277835
50	CEBPB	chr5:93326178-93326440	Hela-S3	cervix:	n/a	chr5:93326350-93326361

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:93333655-93333705	NH-A	brain:	n/a
2	chr5:93349170-93349220	GM19239	blood:	n/a
3	chr5:93327134-93327184	HepG2	liver:	n/a
4	chr5:93137476-93137526	CMK	blood:	n/a
5	chr5:93327134-93327184	HMEC	breast:	n/a
6	chr5:93327134-93327184	GM06990	blood:	n/a
7	chr5:93349170-93349220	NH-A	brain:	n/a
8	chr5:93349170-93349220	HRPEpiC	eye:	n/a
9	chr5:93363467-93363517	SK-N-MC	brain:	n/a
10	chr5:93137476-93137526	NT2-D1	testis:	n/a
11	chr5:93333655-93333705	IMR90	lung:	fetal
12	chr5:93137476-93137526	ovcar-3	ovarian:	n/a
13	chr5:93327134-93327184	HCF	heart:	n/a
14	chr5:93363467-93363517	AG09309	skin:	n/a
15	chr5:93349170-93349220	AoSMC	blood vessel:	n/a
16	chr5:93333655-93333705	GM06990	blood:	n/a
17	chr5:93137476-93137526	NHDF-neo	bronchial:	n/a
18	chr5:93137476-93137526	ECC-1	luminal epithelium:	n/a
19	chr5:93349170-93349220	MCF-7	breast:	n/a
20	chr5:93363467-93363517	HepG2	liver:	n/a
21	chr5:93137476-93137526	GM12892	blood:	n/a
22	chr5:93137476-93137526	HAEpiC	amniotic membrane:	n/a
23	chr5:93137476-93137526	HepG2	liver:	n/a
24	chr5:93333655-93333705	ECC-1	luminal epithelium:	n/a
25	chr5:93333655-93333705	HUVEC	blood vessel:	n/a
26	chr5:93333655-93333705	BE2_C	brain:	n/a
27	chr5:93363467-93363517	BJ	skin:	n/a
28	chr5:93363467-93363517	GM12891	blood:	n/a
29	chr5:93363467-93363517	PrEC	prostate:	n/a
30	chr5:93333655-93333705	HEEpiC	esophagus:	n/a
31	chr5:93363467-93363517	LNCaP	prostate:	n/a
32	chr5:93333655-93333705	MCF10A-Er-Src	breast:	n/a
33	chr5:93363467-93363517	NHDF-neo	bronchial:	n/a
34	chr5:93137476-93137526	NB4	blood:	n/a
35	chr5:93363467-93363517	HL-60	blood:	n/a
36	chr5:93363467-93363517	PANC-1	pancreas:	n/a
37	chr5:93327134-93327184	SK-N-SH	brain:	n/a
38	chr5:93137476-93137526	Hepatocyte	liver:	n/a
39	chr5:93333655-93333705	Caco-2	colon:	n/a
40	chr5:93333655-93333705	RPTEC	kidney:	n/a
41	chr5:93137476-93137526	BE2_C	brain:	n/a
42	chr5:93327134-93327184	HCPEpiC	choroid plexus:	n/a
43	chr5:93327134-93327184	HL-60	blood:	n/a
44	chr5:93137476-93137526	HEK293	kidney:	embryo
45	chr5:93349170-93349220	ECC-1	luminal epithelium:	n/a
46	chr5:93327134-93327184	PANC-1	pancreas:	n/a
47	chr5:93333655-93333705	A549	lung:	n/a
48	chr5:93349170-93349220	Hela-S3	cervix:	n/a
49	chr5:93363467-93363517	HAEpiC	amniotic membrane:	n/a
50	chr5:93349170-93349220	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr5:93300899..93302565-chr5:93320861..93322803,2	MCF-7	breast:
2	chr5:93222617..93225067-chr5:93227445..93229131,2	K562	blood:
3	chr5:93241718..93244108-chr5:93244950..93247843,2	K562	blood:
4	chr5:93222617..93225067-chr5:93227445..93229131,2	K562	blood:
5	chr5:93127282..93128006-chr5:93136216..93137176,2	MCF-7	breast:
6	chr5:93275927..93276429-chr8:43092931..43093789,2	MCF-7	breast:
7	chr5:93366072..93368936-chr5:93371840..93373381,2	K562	blood:
8	chr5:93250600..93251350-chr5:93422167..93422686,2	MCF-7	breast:
9	chr5:93180729..93182562-chr5:93182631..93185240,2	MCF-7	breast:
10	chr5:93136887..93137720-chr5:93230421..93230931,2	MCF-7	breast:
11	chr5:92956324..92956911-chr5:93136722..93137264,2	MCF-7	breast:
12	chr5:93367436..93369479-chr5:93371840..93374615,2	K562	blood:
13	chr5:93244160..93246967-chr5:93249582..93251706,2	MCF-7	breast:
14	chr5:93211648..93213663-chr5:93223328..93224847,2	K562	blood:
15	chr5:93286448..93288914-chr5:93446227..93448641,2	MCF-7	breast:
16	chr5:93236029..93238031-chr5:93238325..93240303,2	MCF-7	breast:
17	chr5:93359990..93361904-chr5:93362067..93364988,2	MCF-7	breast:
18	chr5:93234352..93235271-chr5:93361511..93362065,2	MCF-7	breast:
19	chr5:93241718..93244108-chr5:93244950..93247843,2	K562	blood:
20	chr5:93180729..93182562-chr5:93182631..93185240,2	MCF-7	breast:
21	chr5:92917150..92917848-chr5:93250486..93251539,3	MCF-7	breast:
22	chr5:93236029..93238031-chr5:93238325..93240303,2	MCF-7	breast:
23	chr5:93300899..93302565-chr5:93320861..93322803,2	MCF-7	breast:
24	chr5:93347102..93348867-chr5:93350111..93352553,2	K562	blood:
25	chr5:93361612..93364131-chr5:93365810..93367626,2	MCF-7	breast:
26	chr5:93367436..93369479-chr5:93371840..93374615,2	K562	blood:
27	chr5:93356809..93359800-chr5:93361833..93364201,3	MCF-7	breast:
28	chr5:93244160..93246967-chr5:93249582..93251706,2	MCF-7	breast:
29	chr5:93361612..93364131-chr5:93365810..93367626,2	MCF-7	breast:
30	chr5:93356809..93359800-chr5:93361833..93364201,3	MCF-7	breast:
31	chr5:93227743..93229810-chr5:93246414..93248576,2	K562	blood:
32	chr5:93216595..93218854-chr5:93218865..93220950,2	K562	blood:
33	chr5:93211648..93213663-chr5:93223328..93224847,2	K562	blood:
34	chr5:93227743..93229810-chr5:93246414..93248576,2	K562	blood:
35	chr5:93347102..93348867-chr5:93350111..93352553,2	K562	blood:
36	chr5:92918605..92921388-chr5:93136060..93138274,2	MCF-7	breast:
37	chr5:93133420..93135858-chr5:93140140..93142338,2	MCF-7	breast:
38	chr5:93259705..93262376-chr5:93294800..93297613,2	MCF-7	breast:
39	chr5:93259705..93262376-chr5:93294800..93297613,2	MCF-7	breast:
40	chr5:93136887..93137720-chr5:93230421..93230931,2	MCF-7	breast:
41	chr14:80813126..80813847-chr5:93357357..93357995,2	MCF-7	breast:
42	chr5:93168374..93170848-chr5:93175545..93178313,2	K562	blood:
43	chr5:92932535..92933391-chr5:93137058..93137717,3	MCF-7	breast:
44	chr5:93234352..93235271-chr5:93361511..93362065,2	MCF-7	breast:
45	chr5:92943322..92944183-chr5:93136863..93137431,3	MCF-7	breast:
46	chr5:93168374..93170848-chr5:93175545..93178313,2	K562	blood:
47	chr5:93359990..93361904-chr5:93362067..93364988,2	MCF-7	breast:
48	chr5:92932477..92933445-chr5:93135854..93136694,2	MCF-7	breast:
49	chr5:93366072..93368936-chr5:93371840..93373381,2	K562	blood:
50	chr5:92932499..92933302-chr5:93136722..93137235,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0825-1	chr5:93196375-93199531	ENSG00000251023.1

No data

Variant related genes	Relation type
ENSG00000251023	TF binding region
FAM172A	TF binding region
ENSG00000251023	CpG island
FAM172A	CpG island
ENSG00000251725	chromatin interactions
ENSG00000113391	chromatin interactions
ENSG00000237187	chromatin interactions
ENSG00000175745	chromatin interactions

Extended variants
information (count: 7444 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:7444 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7715555	chr5:93136661-93136662	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372947425	chr5:93136665-93136666	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs571820439	chr5:93136705-93136706	Weak transcription Enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs111898255	chr5:93136722-93136723	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs182035992	chr5:93136791-93136792	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs563520187	chr5:93136937-93136938	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs186633275	chr5:93136938-93136939	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs560589115	chr5:93136976-93136977	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs537376816	chr5:93137154-93137155	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs377606673	chr5:93137249-93137250	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs552239699	chr5:93137294-93137295	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs556921472	chr5:93137301-93137302	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs191743844	chr5:93137326-93137327	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534718564	chr5:93137359-93137360	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs547831429	chr5:93137383-93137384	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs568076500	chr5:93137386-93137387	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs138956460	chr5:93137443-93137444	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs182797573	chr5:93137446-93137447	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs577104159	chr5:93137476-93137477	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs187124422	chr5:93137571-93137572	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs142191506	chr5:93137579-93137580	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs72786662	chr5:93137630-93137631	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs145961767	chr5:93137632-93137633	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs372786647	chr5:93137684-93137685	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560919155	chr5:93137695-93137696	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138544896	chr5:93137766-93137767	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs190035760	chr5:93137841-93137842	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs536669632	chr5:93137862-93137863	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs199971356	chr5:93137875-93137876	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs182104954	chr5:93137892-93137893	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs149238311	chr5:93137954-93137955	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189098095	chr5:93138019-93138020	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78181744	chr5:93138070-93138071	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs528139577	chr5:93138087-93138088	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs9314089	chr5:93138165-93138166	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs553144244	chr5:93138178-93138179	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568038738	chr5:93138224-93138225	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs573295423	chr5:93138256-93138257	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs193036649	chr5:93138264-93138265	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs185380110	chr5:93138271-93138272	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539729089	chr5:93138294-93138295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558736975	chr5:93138325-93138326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76649609	chr5:93138357-93138358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566683952	chr5:93138396-93138397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188499701	chr5:93138408-93138409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144445187	chr5:93138448-93138449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192040177	chr5:93138495-93138496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs5869616	chr5:93138523-93138524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543456502	chr5:93138614-93138615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149842744	chr5:93138625-93138626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Esophageal adenocarcinoma	18519675	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
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:2034 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:93101200-93164200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:93108800-93137400	Weak transcription	Right Ventricle	heart
3	chr5:93109000-93136800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr5:93109200-93159600	Weak transcription	Thymus	Thymus
5	chr5:93109400-93136800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr5:93111400-93142200	Weak transcription	Dnd41	blood
7	chr5:93111400-93159000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr5:93111600-93179800	Weak transcription	Left Ventricle	heart
9	chr5:93111800-93136800	Weak transcription	Liver	Liver
10	chr5:93111800-93136800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr5:93118200-93137400	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr5:93120200-93161800	Weak transcription	Primary B cells from peripheral blood	blood
13	chr5:93125600-93136800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr5:93125600-93136800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr5:93126400-93136800	Weak transcription	Fetal Brain Female	brain
16	chr5:93126600-93136800	Weak transcription	Brain Cingulate Gyrus	brain
17	chr5:93126800-93136800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:93127800-93136800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr5:93127800-93136800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr5:93128000-93136800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:93129800-93136800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr5:93131000-93136800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr5:93131000-93136800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr5:93131000-93136800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr5:93131000-93136800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr5:93131000-93136800	Weak transcription	Psoas Muscle	Psoas
27	chr5:93131000-93137400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr5:93131000-93143800	Weak transcription	Fetal Intestine Large	intestine
29	chr5:93131200-93136800	Weak transcription	Fetal Intestine Small	intestine
30	chr5:93131200-93136800	Weak transcription	Fetal Stomach	stomach
31	chr5:93131200-93136800	Weak transcription	Lung	lung
32	chr5:93131200-93136800	Weak transcription	Pancreas	Pancrea
33	chr5:93131200-93137400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr5:93131200-93139200	Weak transcription	Gastric	stomach
35	chr5:93131200-93148800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr5:93131200-93179200	Weak transcription	Ovary	ovary
37	chr5:93131400-93141200	Weak transcription	Primary T cells from cord blood	blood
38	chr5:93131400-93148600	Weak transcription	Primary B cells from cord blood	blood
39	chr5:93132600-93136800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr5:93132600-93157800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr5:93132800-93140400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:93136000-93137400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr5:93136200-93136800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr5:93136200-93137000	Enhancers	Brain Germinal Matrix	brain
45	chr5:93136200-93137600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr5:93136200-93137600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr5:93136200-93137800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:93136200-93137800	Enhancers	Hela-S3	cervix
49	chr5:93136400-93137000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr5:93136400-93137200	Enhancers	HUES48 Cell Line	embryonic stem cell

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