Variant report

Variant	nsv1065072
Chromosome Location	chr22:30102176-30155245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:699)
CpG islands
(count:1407)
Chromatin interactive
region (count:45)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:699 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30112673-30113047	HepG2	liver:	n/a	n/a
2	ATF3	chr22:30123277-30123446	K562	blood:	n/a	n/a
3	BACH1	chr22:30117117-30117164	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr22:30101958-30102330	GM12878	blood:	n/a	n/a
5	BHLHE40	chr22:30128256-30128610	K562	blood:	n/a	n/a
6	BHLHE40	chr22:30129783-30130011	GM12878	blood:	n/a	n/a
7	BHLHE40	chr22:30112938-30112959	K562	blood:	n/a	n/a
8	BHLHE40	chr22:30122204-30122269	K562	blood:	n/a	n/a
9	BHLHE40	chr22:30123039-30123491	K562	blood:	n/a	chr22:30123301-30123317 chr22:30123298-30123314
10	BHLHE40	chr22:30129772-30130101	K562	blood:	n/a	n/a
11	BRCA1	chr22:30129764-30130130	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr22:30122729-30123043	K562	blood:	n/a	n/a
13	CBX3	chr22:30128277-30128548	K562	blood:	n/a	n/a
14	CCNT2	chr22:30130069-30130217	K562	blood:	n/a	n/a
15	CCNT2	chr22:30122115-30122354	K562	blood:	n/a	n/a
16	CEBPB	chr22:30129437-30129695	K562	blood:	n/a	n/a
17	CEBPB	chr22:30129294-30130046	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr22:30123245-30123541	IMR90	lung:	n/a	n/a
19	CEBPB	chr22:30112775-30113097	HepG2	liver:	n/a	n/a
20	CEBPB	chr22:30129330-30129738	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr22:30123242-30123551	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr22:30153370-30153468	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr22:30123286-30123530	A549	lung:	n/a	n/a
24	CEBPB	chr22:30112795-30113094	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr22:30129409-30129687	K562	blood:	n/a	n/a
26	CEBPB	chr22:30106956-30107195	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr22:30123247-30123550	HepG2	liver:	n/a	n/a
28	CEBPB	chr22:30150747-30150900	HepG2	liver:	n/a	chr22:30150814-30150825
29	CEBPB	chr22:30120445-30120468	IMR90	lung:	n/a	chr22:30120448-30120459
30	CEBPB	chr22:30112810-30112951	HepG2	liver:	n/a	n/a
31	CEBPB	chr22:30123189-30123587	MCF-7	breast:	n/a	n/a
32	CEBPB	chr22:30147179-30147493	HepG2	liver:	n/a	n/a
33	CEBPB	chr22:30150804-30150868	IMR90	lung:	n/a	chr22:30150814-30150825
34	CEBPB	chr22:30147207-30147440	IMR90	lung:	n/a	n/a
35	CEBPB	chr22:30153339-30153502	HepG2	liver:	n/a	n/a
36	CEBPB	chr22:30123253-30123563	K562	blood:	n/a	n/a
37	CEBPB	chr22:30112804-30113093	IMR90	lung:	n/a	n/a
38	CEBPB	chr22:30150702-30150966	HepG2	liver:	n/a	chr22:30150814-30150825
39	CEBPB	chr22:30120332-30120505	A549	lung:	n/a	chr22:30120448-30120459
40	CEBPB	chr22:30120413-30120592	Hela-S3	cervix:	n/a	chr22:30120448-30120459
41	CEBPB	chr22:30150788-30150873	K562	blood:	n/a	chr22:30150814-30150825
42	CEBPB	chr22:30140848-30141119	IMR90	lung:	n/a	n/a
43	CEBPB	chr22:30123279-30123521	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr22:30147153-30147508	K562	blood:	n/a	n/a
45	CEBPB	chr22:30129150-30130110	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr22:30120297-30120612	HepG2	liver:	n/a	chr22:30120448-30120459
47	CEBPB	chr22:30112805-30112998	K562	blood:	n/a	n/a
48	CEBPB	chr22:30150791-30150832	A549	lung:	n/a	chr22:30150814-30150825
49	CEBPB	chr22:30120302-30120606	MCF-7	breast:	n/a	chr22:30120448-30120459
50	CEBPD	chr22:30123286-30123454	HepG2	liver:	n/a	n/a

(count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30116328-30116378	HepG2	liver:	n/a
2	chr22:30117148-30117198	HCT-116	colon:	n/a
3	chr22:30115203-30115253	AoSMC	blood vessel:	n/a
4	chr22:30125642-30125692	LNCaP	prostate:	n/a
5	chr22:30116328-30116378	HepG2	liver:	n/a
6	chr22:30117148-30117198	HCT-116	colon:	n/a
7	chr22:30115203-30115253	AoSMC	blood vessel:	n/a
8	chr22:30125642-30125692	LNCaP	prostate:	n/a
9	chr22:30115203-30115253	GM12878	blood:	n/a
10	chr22:30116319-30116369	SK-N-SH_RA	brain:	n/a
11	chr22:30127118-30127168	GM19239	blood:	n/a
12	chr22:30125353-30125403	SAEC	small airway:	n/a
13	chr22:30119712-30119762	NB4	blood:	n/a
14	chr22:30112403-30112453	SK-N-SH_RA	brain:	n/a
15	chr22:30116328-30116378	MCF10A-Er-Src	breast:	n/a
16	chr22:30116953-30117003	HMEC	breast:	n/a
17	chr22:30115154-30115204	K562	blood:	n/a
18	chr22:30116319-30116369	MCF-7	breast:	n/a
19	chr22:30116953-30117003	SAEC	small airway:	n/a
20	chr22:30117734-30117784	H1-hESC	embryonic stem cell:	embryo
21	chr22:30127118-30127168	Hepatocyte	liver:	n/a
22	chr22:30115348-30115398	ECC-1	luminal epithelium:	n/a
23	chr22:30115203-30115253	BJ	skin:	n/a
24	chr22:30115203-30115253	SK-N-SH_RA	brain:	n/a
25	chr22:30125483-30125533	SAEC	small airway:	n/a
26	chr22:30115203-30115253	HEEpiC	esophagus:	n/a
27	chr22:30125483-30125533	SKMC	muscle:	n/a
28	chr22:30117148-30117198	CMK	blood:	n/a
29	chr22:30125483-30125533	HMEC	breast:	n/a
30	chr22:30116919-30116969	Caco-2	colon:	n/a
31	chr22:30119712-30119762	NHDF-neo	bronchial:	n/a
32	chr22:30125483-30125533	SK-N-SH_RA	brain:	n/a
33	chr22:30127118-30127168	HRPEpiC	eye:	n/a
34	chr22:30122327-30122377	NHBE	bronchial:	n/a
35	chr22:30141053-30141103	HL-60	blood:	n/a
36	chr22:30116953-30117003	HCT-116	colon:	n/a
37	chr22:30115348-30115398	MCF-7	breast:	n/a
38	chr22:30117734-30117784	Hela-S3	cervix:	n/a
39	chr22:30115203-30115253	HUVEC	blood vessel:	n/a
40	chr22:30125483-30125533	Jurkat	blood:	n/a
41	chr22:30127118-30127168	AG04450	lung:	fetal
42	chr22:30129607-30129657	AG04450	lung:	fetal
43	chr22:30116328-30116378	NH-A	brain:	n/a
44	chr22:30116489-30116539	HL-60	blood:	n/a
45	chr22:30116489-30116539	NHBE	bronchial:	n/a
46	chr22:30116037-30116087	LNCaP	prostate:	n/a
47	chr22:30117734-30117784	HL-60	blood:	n/a
48	chr22:30116953-30117003	SK-N-SH_RA	brain:	n/a
49	chr22:30116328-30116378	HCPEpiC	choroid plexus:	n/a
50	chr22:30129607-30129657	ECC-1	luminal epithelium:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30144553..30146905-chr22:30152166..30154338,3	MCF-7	breast:
2	chr22:30123279..30125899-chr22:30126231..30128918,2	K562	blood:
3	chr22:30144553..30146905-chr22:30152166..30154338,3	MCF-7	breast:
4	chr22:30128408..30130433-chr22:30161291..30163799,2	MCF-7	breast:
5	chr22:30148345..30151530-chr22:30155464..30158156,3	MCF-7	breast:
6	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
7	chr22:30118032..30120779-chr22:30154984..30156711,2	K562	blood:
8	chr22:30135111..30137455-chr22:30141470..30144208,2	K562	blood:
9	chr22:30144477..30147071-chr22:30161090..30163905,2	K562	blood:
10	chr22:30139115..30141689-chr22:30143703..30146029,2	K562	blood:
11	chr22:30126165..30128637-chr22:30161660..30163491,2	MCF-7	breast:
12	chr22:30142692..30145269-chr22:30145289..30147345,2	K562	blood:
13	chr22:30096968..30098760-chr22:30102459..30104662,3	MCF-7	breast:
14	chr22:30119899..30121884-chr22:30123778..30126684,2	MCF-7	breast:
15	chr22:30136102..30138464-chr22:30143800..30146252,2	MCF-7	breast:
16	chr22:30139115..30141689-chr22:30143703..30146029,2	K562	blood:
17	chr22:30124714..30127862-chr22:30128538..30131492,3	K562	blood:
18	chr22:30117740..30119771-chr22:30165612..30167453,2	MCF-7	breast:
19	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:
20	chr22:30122754..30125379-chr22:30128810..30131334,3	MCF-7	breast:
21	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
22	chr22:30136102..30138464-chr22:30143800..30146252,2	MCF-7	breast:
23	chr22:30142692..30145269-chr22:30145289..30147345,2	K562	blood:
24	chr22:30151892..30154104-chr22:30162701..30164213,2	MCF-7	breast:
25	chr22:30145045..30147687-chr22:30166151..30168873,2	MCF-7	breast:
26	chr22:30118032..30120779-chr22:30154984..30156711,2	K562	blood:
27	chr22:30123279..30125899-chr22:30126231..30128918,2	K562	blood:
28	chr22:30120187..30123071-chr22:30140004..30142315,2	K562	blood:
29	chr22:30114234..30116768-chr22:30120016..30122557,3	MCF-7	breast:
30	chr22:30135111..30137455-chr22:30141470..30144208,2	K562	blood:
31	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
32	chr22:30120187..30123071-chr22:30140004..30142315,2	K562	blood:
33	chr22:30149066..30150867-chr22:30154689..30156736,2	K562	blood:
34	chr22:30122754..30125379-chr22:30128810..30131334,3	MCF-7	breast:
35	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
36	chr22:30126344..30127866-chr22:30201046..30202629,2	K562	blood:
37	chr22:30127476..30130014-chr22:30183535..30186061,2	MCF-7	breast:
38	chr22:30124714..30127862-chr22:30128538..30131492,3	K562	blood:
39	chr22:30133945..30136337-chr22:30161656..30163853,2	MCF-7	breast:
40	chr22:30119899..30121884-chr22:30123778..30126684,2	MCF-7	breast:
41	chr22:30130941..30133818-chr22:30144985..30147499,2	MCF-7	breast:
42	chr22:30154812..30156577-chr22:30161281..30164280,2	MCF-7	breast:
43	chr22:30097362..30099278-chr22:30100636..30102663,2	K562	blood:
44	chr22:30130941..30133818-chr22:30144985..30147499,2	MCF-7	breast:
45	chr22:30153529..30155692-chr22:30219778..30222690,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZMAT5-1	chr22:30115558-30115703	XLOC_014338
2	lnc-ZMAT5-1	chr22:30115537-30115848	XLOC_014338
3	lnc-ZMAT5-1	chr22:30107809-30107906	XLOC_014338
4	lnc-ZMAT5-1	chr22:30102120-30102223	XLOC_014338
5	lnc-ZMAT5-1	chr22:30115537-30115737	XLOC_014338
6	lnc-ZMAT5-1	chr22:30114214-30114787	NONHSAT084729
7	lnc-ZMAT5-1	chr22:30107802-30107984	XLOC_014338
8	lnc-ZMAT5-1	chr22:30115537-30115756	NONHSAT084729

No data

Variant related genes	Relation type
ENSG00000200976	TF binding region
CABP7	TF binding region
ENSG00000232396	TF binding region
ENSG00000239446	TF binding region
ENSG00000200976	CpG island
CABP7	CpG island
ENSG00000232396	CpG island
ENSG00000239446	CpG island
ENSG00000232396	chromatin interactions
ENSG00000100319	chromatin interactions
ENSG00000100325	chromatin interactions
ENSG00000239446	chromatin interactions
ENSG00000100314	chromatin interactions
ENSG00000200976	chromatin interactions
ENSG00000184076	chromatin interactions
NID1	miRNA target sites
NHLRC3	miRNA target sites

Extended variants
information (count: 2136 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566759565	chr22:30102209-30102210	Enhancers Weak transcription Bivalent Enhancer	lncRNA	n/a	Overlapped CNVs	n/a
2	rs562149109	chr22:30102274-30102275	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs529362477	chr22:30102287-30102288	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs151270241	chr22:30102349-30102350	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs569369634	chr22:30102448-30102449	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533136064	chr22:30102456-30102457	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185918421	chr22:30102513-30102514	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140467535	chr22:30102530-30102531	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs202036413	chr22:30102568-30102569	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533844677	chr22:30102573-30102574	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555491250	chr22:30102574-30102575	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567370443	chr22:30102608-30102609	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538526086	chr22:30102623-30102624	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs59237579	chr22:30102643-30102644	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs555968140	chr22:30102663-30102664	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150401703	chr22:30102760-30102761	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545015267	chr22:30102866-30102867	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553841975	chr22:30102891-30102892	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573534084	chr22:30102892-30102893	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540953099	chr22:30102941-30102942	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182273868	chr22:30102952-30102953	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571538214	chr22:30102953-30102954	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544819689	chr22:30102969-30102970	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562840651	chr22:30102988-30102989	Enhancers Weak transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77228408	chr22:30103051-30103052	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs147655198	chr22:30103137-30103138	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs537574290	chr22:30103150-30103151	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs186167341	chr22:30103172-30103173	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs527552958	chr22:30103177-30103178	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs549022716	chr22:30103226-30103227	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557489876	chr22:30103244-30103245	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141447880	chr22:30103260-30103261	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375179363	chr22:30103282-30103283	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537620109	chr22:30103297-30103298	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543253149	chr22:30103347-30103348	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191013965	chr22:30103366-30103367	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538745111	chr22:30103373-30103374	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559307750	chr22:30103375-30103376	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553776992	chr22:30103413-30103414	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs572088628	chr22:30103454-30103455	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs2530682	chr22:30103476-30103477	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs182845487	chr22:30103519-30103520	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs574323141	chr22:30103547-30103548	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs544470191	chr22:30103600-30103601	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs563107939	chr22:30103685-30103686	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs35921780	chr22:30103701-30103702	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs577669444	chr22:30103704-30103705	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs548685974	chr22:30103706-30103707	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs73390954	chr22:30103747-30103748	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs531148032	chr22:30103797-30103798	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1578 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30095800-30103000	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr22:30096000-30103600	Enhancers	Fetal Brain Male	brain
3	chr22:30096200-30103200	Enhancers	Fetal Brain Female	brain
4	chr22:30096400-30103000	Enhancers	Brain Anterior Caudate	brain
5	chr22:30096400-30103200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr22:30096400-30103600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr22:30096400-30107400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr22:30096600-30103800	Enhancers	Brain Cingulate Gyrus	brain
9	chr22:30097000-30102200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr22:30097000-30106400	Weak transcription	Psoas Muscle	Psoas
11	chr22:30098000-30102800	Weak transcription	Esophagus	oesophagus
12	chr22:30098800-30102400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr22:30098800-30115600	Weak transcription	Right Atrium	heart
14	chr22:30099400-30103600	Enhancers	Brain Germinal Matrix	brain
15	chr22:30099600-30103200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr22:30099600-30103400	Enhancers	Gastric	stomach
17	chr22:30099800-30102200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
18	chr22:30099800-30103000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr22:30100000-30103200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr22:30100200-30102400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr22:30100200-30103200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr22:30100400-30102200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
23	chr22:30100800-30102200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr22:30100800-30102200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr22:30100800-30103600	Enhancers	Brain Substantia Nigra	brain
26	chr22:30101000-30102200	Weak transcription	NH-A	brain
27	chr22:30101000-30102800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr22:30101000-30103200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr22:30101000-30103400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr22:30101000-30103600	Enhancers	Brain Angular Gyrus	brain
31	chr22:30101400-30102200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr22:30101400-30102200	Weak transcription	Spleen	Spleen
33	chr22:30101400-30104800	Weak transcription	HSMMtube	muscle
34	chr22:30101600-30102400	Enhancers	Fetal Muscle Leg	muscle
35	chr22:30101600-30103800	Enhancers	Brain Hippocampus Middle	brain
36	chr22:30102000-30102200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
37	chr22:30102000-30102200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr22:30102000-30102400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
39	chr22:30102000-30102800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr22:30102200-30102400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr22:30102200-30102400	Enhancers	NH-A	brain
42	chr22:30102200-30102600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr22:30102200-30102800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr22:30102200-30102800	Enhancers	Spleen	Spleen
45	chr22:30102200-30103000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr22:30102200-30103000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr22:30102200-30103000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
48	chr22:30102400-30102600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
49	chr22:30102400-30102600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr22:30102400-30102600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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